Biocompatible adhesives and methods of manufacture thereof

ABSTRACT

A biocompatible adhesive is provided comprising one or more water insoluble compounds of structure (1) wherein B is an oligomer derived from a polyester, polyether, polyalkylene glycol, polysilicone or polycarbonate with a MW&lt;10,000 g/mol, Linker L is a urethane, urea bond, or amide bond; Linker L′ is a urethane or urea bond, A is a chain extender of Mw≤3000 g/mol comprising substituted or unsubstituted alkyl, cycloalkyl and/or aromatic groups, W is a terminal adhesive benzene-1,2-diol derivative or a terminal adhesive benzene-1,2,3-diol derivative, m is 0 or 1; and n is 0, 1, 2, 3 or 4; or a cross-linked polymer formed from said compounds. The compound(s) have a Tg lower than 25° C. The biocompatible adhesive is suitable for use without solvent.

This application claims priority to United Kingdom patent application no. 1919026.3 filed Dec. 20, 2019.

FIELD OF THE INVENTION

The invention relates to synthetic degradable biomedical adhesives which bond in wet and dry conditions, such as those encountered during medical procedures.

BACKGROUND

Adhesives capable of bonding in wet environments are well suited for biomedical applications. However, most commercially available adhesives suffer major compromises in bond strength, curing time and/or biocompatibility, rendering them inappropriate for many clinical applications. Conventional adhesives generally require clean, dry surfaces for optimal performance which renders them ineffective for binding in wet environments. Furthermore, the vast majority of conventional adhesives are not biodegradable or resorbable and lack suitable mechanical properties to be used as tissue adhesives or sealants. This has greatly limited the application of surgical adhesives in biomedical applications.

Dental adhesives such as glass ionomer cements (GICs), two-part epoxies and light-cured methacrylate resin systems are generally toxic, slow curing, and require an external light source, acid etching, multiple cure cycles and/other multi-step surface pretreatment techniques. Due to the toxicity and/or extensive preparation required for these materials, they have not been approved for use outside of oral applications where the lack of alternative wet adhesives have necessitated their use [1].

Adhesives which have been approved for clinical use include fibrin, cyanoacrylate, gelatin-resorcin formaldehyde/glutaraldehyde, and PEG-based glues. These adhesive systems all are limited by low bonding under wet conditions and/or poor cytocompatibility [2-9].

PEG-based adhesives, which are extensively used, are relatively non-degradable and are associated with adverse swelling issues which can cause nerve and organ damage [8].

Catechol-containing polymeric adhesives inspired by aquatic, marine mussels are of interest due to the natural ability of mussels to bind to a multitude of surfaces under heavily biofouled conditions. Mussel adhesion is reversible and capable of withstanding fluctuations in temperature and ionic strength [10-12]. The four main components of the mussel adhesive are: 1) acid mucopolysaccharides which act as primers; 2) adhesive proteins consisting mainly of polyphenolic proteins rich in the catechol 3,4-dihydroxyphenylalanine (L-DOPA) and lysine; 3) fibrous proteins that act as an attachment thread between mussel and substrate; and 4) polyphenoloxidase to promote intermolecular cross-linking [13, 14].

Branched PEG and grafted catechol-containing polymer derivatives have demonstrated adhesion to biological tissues, but the requirement for solvents and long curing durations renders them unsuitable for most clinical applications [15-18]. In general, these systems are composed of non-degradable polymers and require the use of solvents which may be toxic and impede curing and bonding of the adhesive. Solvent removal is further required for the adhesives to function optimally and is generally accomplished by evaporation or other means of removal. The lengthy duration of the solvent removal process (on average lasting up to multiple days) is an important consideration when designing biocompatible adhesives [6, 19].

U.S. Pat. No. 8,673,286 discloses poly(alkylene oxide) adhesives using branched (10-20 kDa-PEG)₄ backbones, functionalized with DOPA₄, DOPA-Boc, DOPA₃-Lys₂, DOHA or DOPA with ester or urethane linkages. These adhesives must be solubilized in PBS and mixed in situ by hand in the presence of a water-solubilized oxidant (NaIO₄) prior to use.

PCT Pat. Appl. Publ. No. WO 2017/044896 discloses high molecular weight water soluble adhesives made of linear and branched structures made from PEG or PEGylated polyols, functionalized internally with DOPA using isocyanates. The disclosed formulations require the use of large amounts of filler material, such as dicalcium phosphate, to increase the mechanical properties of the adhesive. The adhesives further include long PEG segments which are non-biodegradable as well as hexamethyl diisocyanate which can produce toxic alkyl diamine biproducts when degraded.

U.S. Pat. No. 8,916,652 discloses branched structures made from PEG-based polyol oligomers. Structures described in the patent are functionalized internally with DOPA, DOPA-Lys, or DOHA using amide/urea linkages. Several disclosed formulations further contain ester or urethane linkages within the branches. All of these disclosed formulations, however, require the use of solvent for application; the adhesives are prepared for use by separately dissolving the polymer and NaIO₄ as a crosslinking agent in PBS and mixing at a ratio of 1:1 before being spread onto the surface using a spray apparatus.

US Pat. Appl. Publ. No. 2010/0137903 discloses substrates (e.g. films, meshes, etc.) which are treated with high molecular weight bioadhesives based on branched PEG oligomers for use in hernia repairs. Application of these adhesives onto substrates requires a curing procedure in which a first oxidant is added to the adherend substrate and then a weight is placed over the adhesive interface and held stationary for at least 1 hour. In some cases, a second application of oxidant is employed. A prolonged application period as described in this application is not practical or possible in most surgical procedures.

U.S. Pat. No. 8,754,285 B2 discloses the synthesis of thin films designed to adhere to a wide assortment of surfaces. The polymer adhesives consist of PCL, PEG and DOPA groups linked through ester and urethane linkages. Although these catechol-containing hydrogels have demonstrated pH-triggered curing and have potential for use as surgical adhesives [20], their complex preparation (constant stirring and careful pH control) limits their practical clinical applications. Furthermore the adhesives disclosed in the patent use toxic solvents, which are of significant concern for in vivo translation. Furthermore, the complexity of this application process is significant, and much more difficult than the current standard of care.

All of the above adhesives suffer from similar disadvantages selected from complex, application strategies involving solvents. Organic solvents are required for application, and spreading and surface penetration strategies may be required. These limitations highlight the need for alternate adhesives which perform in wet conditions; have low toxic reactivity with cells, are easy to process and apply and are biodegradable; and yet have sufficient mechanical properties for given needs. Additionally, for successful clinical entry, the adhesives must be easy and straightforward to use within the confines of a clinical setting and minimally affecting workflow. Multi-step application processes with significant curing times represent a significant burden to clinical workflows and will not be tolerated.

BRIEF SUMMARY

The present disclosure provides:

In a first embodiment, a water insoluble adhesive comprising:

-   -   a compound of structure 1

Structure I

-   -   wherein     -   the compound has a Tg lower than 25° C.;     -   the compound is water insoluble;     -   B is a branched or unbranched oligomer derived from a polyester,         polyether,     -   polyalkylene glycol, polysilicone or polycarbonate with a         MW<10,000 g/mol;     -   Linker L is an urethane, urea bond, or amide bond;     -   Linker L′ is an urethane or urea bond;     -   A is a chain extender of Mw 3000 g/mol comprising substituted or         unsubstituted alkyl, cycloalkyl and/or aromatic groups;     -   W is a terminal adhesive selected from an adhesive         benzene-1,2-diol derivative or an adhesive benzene-1,2,3-triol         derivative;     -   m is 0 or 1; and     -   n is 0, 1, 2, 3 or 4; or     -   a cross-linked polymer produced by cross-linking compounds of         structure 1.     -   2. The water insoluble adhesive of embodiment 1, wherein m is 1         and the adhesive comprises a compound of structure 2

Structure 2

-   -   or     -   a cross-linked polymer produced by cross-linking compounds of         structure 2.     -   3. The water insoluble adhesive of embodiment 2 wherein n is 0         and the adhesive comprises a compound of structure 3

Structure 3

-   -   or     -   a cross-linked polymer produced by cross-linking compounds of         structure 3.     -   4. The water insoluble adhesive of embodiment 2 wherein n is 1         and the adhesive comprises a compound of structure 4

Structure 4

-   -   or     -   a cross-linked polymer produced by cross-linking compounds of         structure 4.     -   5. The water insoluble adhesive of embodiment 2 wherein n is 2         and the adhesive comprises a compound of structure 5

Structure 5

-   -   or     -   a cross-linked polymer produced by cross-linking compounds of         structure 5.     -   6. The water insoluble adhesive of embodiment 2 wherein n is 3         and the adhesive comprises a compound of structure 6

Structure 6

-   -   or     -   a cross-linked polymer produced by cross-linking compounds of         structure 6.     -   7. The water insoluble adhesive of embodiment 2 wherein n is 4         and the adhesive comprises a compound of structure 7

Structure 7

-   -   or     -   a cross-linked polymer produced by cross-linking compounds of         structure 7.     -   8. The water insoluble adhesive of any of the preceding         embodiments wherein the compound has a Tm equal to or greater         than 37° C.     -   9. The water insoluble adhesive of any of the preceding         embodiments wherein B has a Mw<5,000 g/mol, preferably <3,000         g/mol.     -   10. The water insoluble adhesive of any of the preceding         embodiments, wherein B is hydrolysable or enzyme degradable.     -   11. The water insoluble adhesive of any any of the preceding         embodiments, wherein L and/or L′ is hydrolysable or enzyme         degradable.     -   12. The water insoluble adhesive of any any of the preceding         embodiments wherein B is an oligomer derived from         polycaprolactone, polydimethylsiloxane, polypropylene glycol or         polyhexamethylene carbonate, preferably polycaprolactone.     -   13. The water insoluble adhesive of any of the preceding         embodiments wherein A is a substituted or unsubstituted alkyl         group.     -   14. The water insoluble adhesive of embodiment 13 wherein A is         methyl hexanoate.     -   15. The water insoluble adhesive of any of the preceding         embodiments wherein A has a MW<200 g/mol.     -   16. The water insoluble adhesive of any of the preceding         embodiments wherein W is a 4-alkylbenzene-1,2-diol derivative or         a 5-alkylbenzene-1,2,3-triol derivative.     -   17. The water insoluble adhesive of any of the preceding         embodiments wherein W has a structure selected from:

-   -   wherein R is present or absent and when present is a C1-C6 alkyl         group or C1-C6 alkene optionally substituted with OH, NH.     -   18. The water insoluble adhesive of any one of embodiments 1-17         comprising a compound having m is 1 and n is 0 and another         compound having m is 1 and n is 0, 1, 2, 3 or 4.     -   19. The water insoluble adhesive of any one of embodiments 1-17         comprising a compound having m is 1 and n is 0 and another         compound having m is 1 and n is 1.     -   20. The water insoluble adhesive of any of the preceding         embodiments consisting or consisting essentially of one or more         compounds of structure 1, optionally a single compound of         structure 1.     -   21. The water insoluble adhesive of any one of embodiments 1-19,         further comprising one or more of a filler, a cross-linking         agent, a porogen and an additive.     -   22. The water insoluble adhesive of embodiment 21, wherein the         adhesive comprises a compound of structure 1 and a cross-linking         agent.     -   23. The water insoluble adhesive of embodiment 22 wherein the         cross-linking agent promotes covalent cross-linking of the         terminal adhesive with another terminal adhesive and/or of the         terminal adhesive with tissue.     -   24. The water insoluble adhesive of embodiment 22 or 23, wherein         the cross-linking agent is selected from sodium carbonate and/or         iron(III) salts.     -   25. The water insoluble adhesive of any one of embodiments         21-24, wherein the adhesive comprises between 0.1 and 10 percent         by weight cross-linking agent, based on the weight of the         adhesive, preferably between 0.5 and 5 percent by weight         cross-linking agent, based on the weight of the adhesive.     -   26. The water insoluble adhesive of any one of embodiments 1-19,         wherein the adhesive comprises a cross-linked polymer prepared         by combining one or more compounds of structure 1 with a         cross-linking agent or a curing agent, preferably selected from         sodium carbonate and/or iron(III) salts.     -   27. The water insoluble adhesive of any of the preceding         embodiments further comprising a biocompatible polymer or         oligomer, preferably a biodegradable polyester, more preferably         polycaprolactone.     -   28. The water insoluble adhesive of embodiment 27, wherein the         adhesive comprises 5-95%, preferably between 30-70%, by weight         compounds of structure 1 or a cross-linked polymer produced by         cross-linking compounds of structure 1; and 5-95%, preferably         30-60% by weight of the biocompatible polymer or oligomer.     -   29. The water insoluble adhesive of any of the preceding         embodiments having an adhesive strength greater than 25 KPa         under compression, tensile, or tensile lap shear testing.     -   30. The water insoluble adhesive of any of the preceding         embodiments having a viscosity sufficient to be expelled out of         a syringe at a temperature of at least 20° C.     -   31. The water insoluble adhesive of any of the preceding         embodiments having a viscosity sufficient to be expelled from a         needle having a gauge between 7 gauge to 33 gauge or more         specifically 16 gauge, 17 gauge or 21 gauge at a temperature of         at least 20° C.     -   32. The water insoluble adhesive of any of the preceding         embodiments wherein the adhesive has free-flowing behavior at a         temperature of at least 20° C.     -   33. The water insoluble adhesive of any one of embodiments 1-29,         wherein the compound is an amorphous solid.     -   34. A composition comprising a water insoluble adhesive as         provided herein and a biological agent, pharmaceutical agent or         diagnostic agent covalently bound or complexed to the compound         or entrapped within the adhesive.     -   35. A method of adhering a first surface and a second surface         comprising: applying the adhesive of any one of embodiments 1-33         to at least a portion of the first surface; and bringing at         least a portion of the second surface into contact with the         adhesive.     -   36. The method of embodiment 35, further comprising applying an         adhesive according to any one of embodiments 1-33 to the second         surface.     -   37. The method of embodiment 35 or 36 wherein at least one of         the surfaces is a wet surface, saline surface and/or a surface         contaminated with proteins and/or biomolecules.     -   38. The method of any one of embodiments 35-37 wherein the first         surface comprises soft tissue and the second surface comprises         hard tissue or an implant or device.     -   39. The method of any one of embodiments 35-37 wherein both         surfaces are soft tissue.     -   40. The method of any one of embodiments 35-37 wherein the first         surface comprises hard tissue and the second surface is a         surface of an implant or device.     -   41. The method of any one of embodiments 35-37 wherein both         surfaces are hard tissue.     -   42. A method of adhering a substance to blood or components         thereof comprising contacting the substance and the blood or         components thereof with an adhesive according to any one of         embodiments 1-33.     -   43. The method of any one of embodiments 35 to 42 further         comprising applying an external energy source to the adhesive         and/or at least one of the first and second surface to enhance         adhesion or application.     -   44. The adhesive of embodiment 2 wherein the compound is         prepared by reacting a first isocyanate group of a diisocyanate         having a substituted or unsubstituted alkyl-derived chain         extender, a substituted or unsubstituted cycloalkyl-derived         chain extender, or a substituted or unsubstituted benzyl-derived         chain extender between the two isocyanate groups     -   with terminal amino or alcohol groups of an oligomer having at         least two terminal amino or alcohol groups and     -   reacting a second isocyanate of the diisocyanate molecule with         an amine group, alcohol group or carboxy group present on an         alkyl chain of a 4-alkylbenzene-1,2-diol derivative or a         5-alkylbenzene-1,2,3-triol derivative.     -   45. The adhesive of embodiment 44 wherein the oligomer is an         oligomer derived from a polyester, polyether, polyalkyloxide,         polysilicone or polycarbonate.     -   46. The adhesive of embodiment 45 wherein the oligomer chain is         an oligomer derived from polycaprolactone, polydimethylsiloxane,         polypropylene glycol, or polyhexamethylene carbonate.     -   47. The adhesive of any one of embodiments 44-46 wherein the         diisocyanate molecule is selected from the group consisting of:

-   -   48. The adhesive of any one of embodiment 44-47 wherein the         4-alkylbenzene-1,2-diol derivative or a         5-alkylbenzene-1,2,3-triol derivative is selected from the group         consisting of:

-   -   In other embodiments, there is provided any novel water         insoluble compound of structure 1 as provided above or as         exemplified in the present description.

BRIEF DESCRIPTION OF THE DRAWINGS

These and other features of the preferred embodiments of the invention will become more apparent in the following detailed description in which reference is made to the appended drawings wherein:

FIG. 1 shows a representation of a device consisting of a flexible backbone polymer and an adhesive stabilizing a bone fracture, reflecting a suitable application of adhesives taught herein;

FIG. 2 shows compound of Structure 1 according to an embodiment;

FIG. 3 shows compound of Structure 2 according to an embodiment;

FIG. 4 shows compound of Structure 3 according to an embodiment;

FIG. 5 shows compound of Structure 4 according to an embodiment;

FIG. 6 shows compound of Structure 5 according to an embodiment;

FIG. 7 shows compound of Structure 6 according to an embodiment;

FIG. 8 shows compound of Structure 7 according to an embodiment;

FIG. 9 shows compound of Structure 8 according to an embodiment;

FIG. 10 shows an exemplary list of commercially available monomers or oligomers that may be used for the preparation of the compounds of the present disclosure according to an embodiment;

FIG. 11 shows an exemplary list of polyalcohols and sugar alcohols that may be used as a starting point for the preparation of the oligomer according to an embodiment;

FIG. 12 shows general preparation of polycaprolactone pentaol oligomers according to an embodiment;

FIG. 13 shows general preparation of polycaprolactone hexaol oligomers according to an embodiment;

FIG. 14 shows the general preparation of a PPG pentaol oligomers according to an embodiment;

FIG. 15 shows an exemplary list of diisocyanate molecules that may be used for the preparation of the compounds of the present disclosure according to an embodiment;

FIG. 16 shows an exemplary list of 4-alkylbenzene-1,2-diol derivative and a 5-alkylbenzene-1,2,3-triol derivative that may be used for the preparation of the compounds of the present disclosure according to an embodiment;

FIG. 17 shows a generalized reaction scheme for the synthesis of difunctional PCL adhesives according to an embodiment;

FIG. 18 shows a method for the activation of dopamine hydrochloride into free dopamine according to an embodiment;

FIG. 19 shows a generalized reaction scheme for the synthesis of trifunctional PCL adhesives according to an embodiment;

FIG. 20 shows a generalized reaction scheme for the synthesis of tetrafunctional PCL adhesives according to an embodiment;

FIG. 21 shows a generalized reaction scheme for the synthesis of penta-functional PCL adhesives via arabitol according to an embodiment;

FIG. 22 shows a generalized reaction scheme for the synthesis of hexafunctional PCL adhesives via tetrakis(hydroxymethyl)oxydipropanol according to an embodiment;

FIG. 23 shows a generalized reaction scheme for the synthesis of difunctional PDMS adhesive according to an embodiment;

FIG. 24 shows a generalized reaction scheme for the synthesis of difunctional PPG adhesive according to an embodiment;

FIG. 25 shows a generalized reaction scheme for the synthesis of difunctional PCN adhesive according to an embodiment;

FIG. 26 shows an example of the use of Adhesive 2a to secure a piece of polymer film to porcine skin according to an embodiment;

FIG. 27 shows an example of the use of Adhesive 2a to secure bone to bone according to an embodiment;

FIG. 28 shows an example of the use of Adhesive 2a to secure porcine skin to bone according to an embodiment;

FIG. 29 shows an example of Adhesive 2a to secure porcine skin to skin according to an embodiment;

FIG. 30 shows an example of Adhesive 2a to secure porcine bone to a polymeric film and porcine skin to the same polymeric film according to an embodiment;

FIG. 31 shows failure modes for samples incubated in physiological fluids for 24 h according to an embodiment; and

FIG. 32 shows the affect of residual solvent on the adhesive strength of Adhesive 5 according to an embodiment.

DETAILED DESCRIPTION

For further clarity, the following terms are defined:

Wet conditions encompass environments which include, but are not limited to, water, water with proteins and/or salts and/or blood and/or other biological macromolecules.

Physiological conditions refer to wet conditions at pH 7.4±0.3 and temperature of 37.5±3° C.

Water insoluble is defined as the ability of a material to resist dissolution and/or the formation of a heterogenous mixture when a solvent-free material is mixed with water in concentrations greater than 0.5 wt/wt % at physiological temperatures (37.5±3° C.). Visible particles of the materials will remain separate and heterogeneous as a solid or gel when the material is hand mixed in water at a concentration of 0.5 wt/wt % at physiological temperatures (37.5±3° C.).

Crosslinking is defined as the formation of a chemical bond, inclusive of covalent bonding and chelation, between two existing macromolecules (for example: adhesive-adhesive crosslinking, adhesive-protein crosslinking).

Curing is defined as the chemical process of converting a macromolecule into a higher molecular weight polymer via crosslinking reactions.

Setting is defined as an irreversible change in the state of a material, from flowable to rigidified, which occurs during curing.

Implant is defined as any material that is designed to function in contact with the human body.

Tm (Melting temperature) is defined as the temperature (or temperature range) at which a well defined first order transition occurs, as determined by an endothermic event in a differential scanning calorimetry thermogram. If there is no such transition, as is common for amorphous materials, Tm will be defined by the beginning of the substance's ability to flow or spread under an applied force (i.e., temperature within the linear viscoelastic region on a stress-sweep viscoelastic curve at which the viscous modulus>elastic modulus (tan δ>1)).

Tg (Glass transition temperature) is defined as the temperature (temperature range) where the polymer transitions from a hard, glassy material to a soft, rubbery material as determined by changes in the heat capacity (Cp), reversible heat flow curves, and material rigidity or hardness obtained from differential scanning calorimetry, dynamic mechanical assessment and needle penetrometer or indentation experiments, respectively.

In the present disclosure, soft tissue refers to connective and/or fatty and/or fibrous soft tissues and/or any organ tissue consisting primarily of low calcified content relative to biomolecule content (e.g. collagens, glycosamino glycans, elastin, etc.). Soft tissues connect, surround, or support bones, organs and other structures in the body. In one embodiment, soft tissues refer in particular to sub-epidermal fatty and/or fibrous tissues. Examples of soft tissues include tendons, muscles, skin, ligaments, nerves, vessels, fascia, fibrous tissues and synovial membranes. In another embodiment soft tissues make up the protein base structures of vital organs such as the heart, blood vessels, intestines, etc.

In the present disclosure, hard tissues are mineralized and rigid tissues containing significant amounts of hydroxyapatite. Examples of hard tissues include bone, enamel, dentin and cementum.

The present disclosure provides an adhesive that may be used to glue or secure hard tissue to hard tissue, hard tissue to implant, hard tissue to soft tissue, soft tissue to soft tissue, soft tissue to implant or implant to implant.

The use of structures described in the present disclosure may eliminate or reduce the need to use staples, sutures, tacks, screws or the like to secure or repair damaged tissues or to secure implants or devices within the body.

Many previously described adhesives are comprised of polymeric chains that are decorated with periodic or randomly distributed branching side chains containing adhesive functional groups. This contributes to high intermolecular bonding (requiring solvents to assist with application and surface wetting) and poor accessibility of adhesive functional groups to the substrates where adhesion is desired.

Adhesives described in the present disclosure when compared to known bioadhesives may be characterized by a rapid high degree of surface wetting/adhesion in a biological environment, easy adherence and retention of the water insoluble adhesive to substrates, and/or elimination of solvent requirement. Such biological environment may reflect the constraints of biological elements (protein, aqueous fluids, temperature, fatty tissue, bony tissue, cells, etc.).

The present disclosure describes water insoluble adhesive compounds consisting of short linear or short branched oligomer chains capped only at their terminal ends with phenyl moieties with two or three hydroxyl groups acting as adhesive moieties as well as cross-linked polymers prepared from these compounds. The oligomer chains may have a MW between 50 and 10,000 g/mol, in other embodiments, between 50 g/mol, 100 g/mol, 500 g/mol or 1000 g/mol and 5,000 g/mol, in other embodiments between 50 g/mol, 100 g/mol, 500 g/mol or 1000 g/mol and 3,000 g/mol. The water insoluble adhesive may be prepared in such way that it will degrade over a period of time when exposed to biological conditions. Alternatively, the water insoluble adhesive may be non-degradable when exposed to biological conditions.

The present disclosure provides water insoluble adhesives which are biocompatible and non-toxic; wherein biocompatible refers to a material which does not induce an observable biological response (e.g. immunological) upon contact with cellular, tissue or other bodily fluids/components [21], and non-toxic refers to a material which does not have an observable negative effect on cell viability. Furthermore, when the compounds of the water insoluble adhesive are tailored to be degradable, the degradation products are biocompatible and non-toxic.

Having adhesive moieties at the terminal ends, while not bound by theory, the compounds of the present disclosure allow the adhesive moieties to preferentially orient to the substrate surface with minimal steric hindrance, and therefore rapid adhesion. Terminal functionalization of adhesive moieties onto the oligomeric backbone may also allow structural control, as many internally functionalized block or grafted polymers have adhesive moieties randomly oriented off of the backbone. Terminal grafting may also reduce the viscosity of the adhesives, as their bulk disrupts packing, reducing intermolecular forces.

Suitably, the oligomers have a MW<10,000 g/mol, preferably less than <5,000 g/mol or <3,000 g/mol. The use of oligomers with a a Mw<5,000 g/mol, and especially a Mw<3000 g/mol greatly reduces intermolecular interactions associated with them due to smaller size and reduced cumulative forces between oligomers. The reduction in intermolecular interactions between the oligomers of the compound of structure 1 may allow the adhesive of the present disclosure to be prepared without the use of a solvent resulting in faster setting/curing, low/no toxicity and improved usability of the adhesive, as solvent has been reported to interfere with adhesive bonding and presents its own toxicity concerns [22-25]. In some embodiments, the oligomer suitable has a molecular weight >50 g/mol, >100 g/mol, >300 g/mol or greater than 500 g/mol.

It is well accepted that adhesives formulated for use in biomedical applications ideally may have some or many of the following characteristics [26-31]:

-   -   bond rapidly or on demand when in contact with a surface     -   cure in a controllable manner     -   work over a suitable range of temperatures     -   adhere to materials without the necessity of pre-treatment or         cleaning     -   exhibit adhesion strength which is maintained over the duration         of the desired application     -   have strong bonding and curing strength     -   are biodegradable     -   obviate the need for a solvent     -   have no smell     -   achieve desirable aesthetic properties     -   are easy to work with and easy to apply     -   easy to incorporate a catalyst to achieve curing, or cures         without catalyst are easy and inexpensive to manufacture     -   work well in wet, dry and situations where contaminants may be         present.

Depending on the structure, the Mw, and the formulation of the compounds of present disclosure, the adhesives described in the present disclosure may have at least one of the criteria listed above.

Water Insoluble Adhesives

According to an embodiment, an adhesive is described. The water insoluble adhesive comprises, consists of or consists essentially of a compound of structure 1 (FIG. 2 ) wherein B is an oligomer, Linker L is a urethane, urea bond, or amide bond; Linker L′ is a urethane or urea bond, A is a chain extender, W is a terminal adhesive moiety, m is 0 or 1; and n is 0, 1, 2, 3 or 4.

Water insolubility can be rendered by assembling an adhesive using B and A components which are themselves water insoluble. Alternatively, water insolubility can be rendered by assembling an adhesive using B and A components which are themselves water soluble but which, upon reaction, undergo increases in their hydrophobic character due to reactive conversion of some or all of the water-soluble functional groups (such as hydroxyl or amine groups.).

According to an embodiment, the compound of structure 1 has m=1 resulting in the compound of structure 2 (FIG. 3 ).

According to an embodiment, the compound of structure 1 has m=1 and n=0 resulting in the compound of structure 3 (FIG. 4 ).

According to an embodiment, the compound of structure 1 has m=1 and n=1 resulting in the compound of structure 4 (FIG. 5 ).

According to an embodiment, the compound of structure 1 has m=1 and n=2 resulting in the compound of structure 5 (FIG. 6 ).

According to an embodiment, the compound of structure 1 has m=1 and n=3 resulting in the compound of structure 6 (FIG. 7 ).

According to an embodiment, the compound of structure 1 has m=1 and n=4 resulting in the compound of structure 7 (FIG. 8 ).

Alternatively, according to an embodiment, the compound of structure 1 has m=0 resulting in the compound of structure 8 (FIG. 9 ).

Block B is an oligomer having a MW between 50 g/mol and 5,000 g/mol, In various embodiments, between 50 g/mol, 100 g/mol or 500 g/mol and 2000 g/mol, 3000 g/mol or 5000 g/mol. Preferably, the oligomer may have a Mw<3,000 g/mol. The Block B may be derived from any suitable biocompatible polymers such as, but not limited to, fluoropolymers, polyesters, polyethers, polyalkyloxide, polyurethanes, polyamides, polysilicone, polycarbonate, or polysaccharides selected such that the compound of structure 1 is water insoluble. According to an embodiment, the Block B is an oligomer derived from polycaprolactone, polydimethylsiloxane, polypropylene glycol or polyhexamethylene carbonate. As used herein, an oligomer “derived from” an identified polymer retains the essential structure and activity of the polymer despite any modifications thereto. In various embodiments, the oligomer is selected from the identified biocompatible polymers.

According to an embodiment, the compound of structure 1 may have a Block B which is either hydrolysable or enzyme degradable under physiological conditions. Alternatively, the Block B may be non-degradable under physiological conditions.

Block B may have a finite number of branches resulting in compounds of Structure 1 or Structure 2 or more particularly compounds of Structure 4, Structure 5, Structure 6 or Structure 7. Alternatively, Block B may be linear resulting in compounds of Structure 3.

According to an embodiment, Block B may be derived from small molecules such as monomers, dimers or trimers. Such monomers, dimers and trimers may be derived from polyhydric alcohols including but not limited to trimethylolpropane, glycerol and pentaerythritol; or from their alkoxylated derivatives.

According to an embodiment, the water insoluble adhesive of the present disclosure may be a compound of structure 8 for which Block B is absent.

Linker L is a urethane bond, a urea bond or an amide bond and Linker L′ is either a urethane bond or a urea bond. According to an embodiment, the compound of structure 1 may be designed to render Linker L and/or Linker L′ hydrolysable or enzyme degradable. Alternatively, the Linker L and/or Linker L′ may be non-degradable under physiological conditions.

Block A is a chain extender comprising substituted or unsubstituted alkyl, cycloalkyl and/or aromatic groups. Block A has a Mw between 20 and 3000 g/mol in some embodiments, between 20 and 65 g/mol, 100 g/mol, 200 g/mol, 500 g/mol, 1000 g/mol or 2000 g/mol. According to an embodiment, Block A is a substituted or unsubstituted alkyl group. According to an embodiment, Block A is a substituted alkyl group, wherein one or more of the hydrogens on the alkyl are replaced, introducing branching. According to an embodiment, Block A may be substituted with C1-C6 carboxylate group. According to another embodiment, Block A is a methyl hexanoate or ethyl hexanoate.

Block W is a terminal adhesive moiety having a phenyl with at least two hydroxyl groups. According to an embodiment, Block W is a terminal adhesive moiety derived from benzene-1,2-diol derivative or benzene-1,2,3-triol derivative. Biologically derived and inspired molecules containing benzene-1,2-diol or benzene-1,2,3-triol derivatives have strong and durable adhesion to various substrate surfaces including wet surfaces. These characteristics are advantageous for the preparation of adhesive molecules for biomedical applications. According to an embodiment, Block W may be a 4-alkylbenzene-1,2-diol derivative. Alternatively Block W may be a 5-alkylbenzene-1,2,3-triol derivative. According to an embodiment, Block W may have a structure selected either Structure 9 or Structure 10 wherein R may be present or absent. When R is present, R may be a C1-C6 alkyl group or C1-C6 alkene optionally substituted with OH, NH or C1-C6 alkyl.

According to some embodiments, the water insoluble adhesives described in the present disclosure comprise a compound suitably have a Tg lower than or equal to 25° C., in one embodiment lower than or equal to 20° C. According to an embodiment, the water insoluble adhesives may have a viscosity sufficient to be expelled out of a syringe at a temperature of at least 20° C. Alternatively, the adhesive may have a viscosity sufficient to be expelled from a needle having a gauge between 7 gauge to 33 gauge or more specifically 16 gauge, 17 gauge or 21 gauge at a temperature of at least 20° C. and less than 50° C. According to another embodiment, the adhesive of the present disclosure may have a free-flowing behavior at a temperature of at least 20° C.

According to an embodiment, the water insoluble adhesives described in the present disclosure may have an adhesive strength greater than 10 kPa under compression, tensile, or tensile lap shear testing. According to other embodiments, the adhesives described in the present disclosure may have an adhesive strength greater than 25 kPa, 50 kPa, greater than 75 kPa or greater than 100 kPa under compression, tensile, or tensile lap shear testing. Adhesives according to disclosed embodiments that have an adhesive strength between 10 kPa and 25 kPa may have particular utility in applications where it is beneficial to have an adhesive that is relatively flexible, including applications involving the adhesion of soft tissues and, in particular, skin.

According to an embodiment, the water insoluble adhesives of the present disclosure may comprise a plurality of compounds derived from the compound of structure 1 with additional admixture(s) whose function may include directly enhancing the adhesive performance (for example, but not limited to polymers, crosslinking agents, fillers and porogens), and/or to provide combination products with further value add (for example, but not limited to drugs, fillers, therapeutics, regenerative materials or other compounds).

According to an embodiment, the water insoluble adhesives of the present disclosure may comprise a plurality of compounds derived from the compound of structure 1. The water insoluble adhesives may comprise a compound of structure 1 having m=0 and another compound of structure 1 having m=1 and n is either 0, 1, 2, 3 or 4 e.g., the water insoluble adhesives may comprise a compound of structure 1 having m=0 and another compound of structure 1 having m=1 and n is 0.

According to an embodiment, the water insoluble adhesives of the present disclosure may comprise a compound of structure 1 having m=1 and n=0 and another compound of structure 1 having m=1 and n is 0, 1, 2, 3 or 4. More particularly, the water insoluble adhesives may comprise a compound of structure 1 having m=1 and n=0 and another compound of structure 1 having m=1 and n=1. According to another embodiment, the water insoluble adhesives of the present disclosure may consist or consist essentially of compounds of structure 1.

According to an embodiment, the water insoluble adhesives of the present disclosure may further comprise a crosslinking agent or a curing agent. In order to achieve a desirable mechanical property and desired setting speed, in some embodiments, the water insoluble adhesive may benefit from the inclusion of crosslinking agents or curing agents. In one embodiment, the setting speed is ≤5 hours. In another embodiment, the setting speed is ≤2 hours. In another embodiment, the setting speed is ≤60 minutes. In another embodiment, the setting speed is ≤15 minutes. In another embodiment, the setting speed is ≤5 minutes. In another embodiment, the setting speed is ≤2 minutes. In another embodiment, the setting speed is ≤1 minute. In another embodiment, the setting speed is ≤30 seconds. In another embodiment, the setting speed is ≤10 seconds. The use of such agents may improve the rigidity and cohesive strength of the adhesives while reducing creep and deformation. 4-alkylbenzene-1,2-diol derivative or a 5-alkylbenzene-1,2,3-triol derivative may be chelated with the use of suitable complexing agents (e.g. Fe(III) salts), and/or irreversibly crosslinked via the use of oxidants, light, basic pH, and enzymes. In some embodiments, the compounds of Structure 1 may have a lower Tg or melting point than the operational temperature. Under such conditions, a curing agent or crosslinking agent is useful to rigidify the adhesives, providing increased cohesive strength. When a crosslinking agent such as an oxidant or a chelating agent is included within the water insoluble adhesive, it may promote covalent crosslinking of the catechol groups with other catechols and/or tissue.

According to an embodiment, the adhesive of the present disclosure may further comprise a biological agent, pharmaceutical agent or diagnostic agent covalently bound or complexed to the compound or entrapped within the adhesive. This could include a drug, protein, enzyme, combination, diagnostic reagent, regenerative material or biosensor. The agent may either diffuse out through the adhesive or be released as the adhesive degrades, or be retained and remain as an active sensor if the adhesive is not degradable.

According to an embodiment, the water insoluble adhesives described in the present disclosure comprise compounds of structure 1 having a Mw<5,000 g/mol and a Tg lower than 20° C. rendering optional the use of a solvent; alternatively the water insoluble adhesive of the present disclosure comprises compounds of structure 1 having a Mw<5,000 g/mol and a Tg lower than 20° C. rendering optional the use of a solvent; and alternatively the water insoluble adhesive of the present disclosure comprises compounds of structure 1 having a Mw<3,000 g/mol and a Tg lower than 20° C. rendering optional the use of a solvent. According to another embodiment, the water insoluble adhesives of the present disclosure may be solvent free.

The solvent-optional or solvent-free nature of the water insoluble adhesive of the present disclosure is advantageous as numerous solvents are known to be toxic and may impede with the bonding of the adhesive to the substrate and may even interfere with the crosslinking and curing process if crosslinking agents or curing agents are used. For example, it is known that adhesives dissolved in solvents typically have reduced cohesive and adhesive properties and rely on diffusion or evaporation of the solvent for improved mechanical performance. Depending on the environment and the nature of the solvent, this diffusion or evaporation of the solvent may be on the order of minutes, hours, days or even longer periods of time. Solvents have been known to cause toxicity or other undesirable effects including intoxication and strong odors [31-32]. Furthermore, using a water insoluble adhesive that does not require a solvent is advantageous for biomedical applications as it alleviates the need for the solvent to evaporate, diffuse or be removed by another mechanism, which are frequent requirements when an adhesive system includes a solvent. The latter events are usually accomplished over an extended time period that may occur over hours or even multiple days, creating very long setting times and limiting the biomedical applications and use of said adhesive formulations.

Methods of Preparing Water Insoluble Adhesives

According to an embodiment, a method of preparing the compound of structure 1 is provided. The method comprises the steps of:

-   -   1. reacting an amino or alcohol group present at each of at         least two end portions of an oligomer with one of two isocyanate         groups of a diisocyanate molecule. The diisocyanate has a         substituted or unsubstituted alkyl-derived chain extender, a         substituted or unsubstituted cycloalkyl-derived chain extender,         or a substituted or unsubstituted benzyl-derived chain extender         sandwiched between the two isocyanate groups;     -   2. reacting the second isocyanate of the diisocyanate molecule         with an amine group, alcohol group or carboxy group present on         an alkyl chain of a 4-alkylbenzene-1,2-diol derivative or a         5-alkylbenzene-1,2,3-triol derivative.

According to another embodiment, a method of preparing the compound of structure 8 is provided. The method comprises the step of reacting each isocyanate group of a diisocyanate with an amine group, alcohol group or carboxy group present on an alkyl chain of a 4-alkylbenzene-1,2-diol derivative or a 5-alkylbenzene-1,2,3-triol derivative. The diisocyanate has a substituted or unsubstituted alkyl-derived chain extender, a substituted or unsubstituted cycloalkyl-derived chain extender, or a substituted or unsubstituted benzyl-derived chain extender between the two isocyanate groups.

According to an embodiment, the oligomer backbone has a Mw of about <10,000 g/mol, <5,000 g/mol or <3,000 g/mol. The oligomer may be non-degradable. Alternatively, the oligomer may be hydrolysable or enzyme degradable under physiological conditions. The oligomer may be branched or unbranched and may be derived from any suitable water insoluble polymer or a soluble polymer that in combination with block A yields a water insoluble compounds of structure 1 that is currently used in implant devices and known to those skilled in the art, such as, but not limited to, fluoropolymers such as PTFE and ETFE, polyethers, polyesters (PLA, PGA, PCL), polyalkyloxide (PEG, PPG), polyurethanes, polyamides, polysilicone (PDMS), polycarbonate (PCN), polyketones (PK), polyacetals (POM), polyolefins or polysaccharides (chitin, chitosan). More, particularly, the oligomer may be derived from a polyester, polyether, polyalkyloxide, polysilicone or polycarbonate. In a preferred embodiment, the oligomer may be derived from polycaprolactone, polydimethylsiloxane, polypropylene glycol, or polyhexamethylene carbonate. While the term oligomer is used, in some embodiments, there are no repeating units. i.e. B comprises a single monomer unit, which was the essential structure and activity of an identified polymer.

According to an embodiment, the oligomer may be linear, resulting in compounds of Structure 3. Alternatively, the oligomer may be branched resulting in compounds of Structure 4, Structure 5, Structure 6 or Structure 7.

According to an embodiment, the oligomer may be selected from commercially available oligomers. FIG. 10 is an exemplary list of commercially available oligomers that may be used for the preparation of the compounds of the present disclosure. Alternatively, the oligomers may be prepared by a skilled person using common general knowledge in the field of polymer chemistry [32]. FIG. 11 shows non-limiting examples of sugar alcohols that may be used as a starting point for the preparation of the oligomer. FIG. 12 and FIG. 13 show examples of the general preparation of polycaprolactone pentaol and hexaol oligomers. FIG. 14 shows an example of the general preparation of PPG pentaol oligomers.

According to an embodiment, the diisocyanate molecule may be selected from the group shown in FIG. 15 .

According to an embodiment, the 4-alkylbenzene-1,2-diol derivative or a 5-alkylbenzene-1,2,3-triol derivative may be selected from the group shown in FIG. 16 . This class of compounds have been known for their adhesion properties and are suitable for the synthesis of adhesive molecules. According to another embodiment, the preferred 4-alkylbenzene-1,2-diol derivative is dopamine and the preferred 5-alkylbenzene-1,2,3-triol derivative is 3,4,5-trihydroxyphenethylamine.

In some embodiments, the adhesive includes cross-linked structures. Biocompatible crosslinking agents are known to persons of skill in the art. Suitable crosslinking agents can include inorganic oxidants (Na₃VO₄ and tetrabutylammonium (meta)periodate (TBAP)), an organic or inorganic bases ((Na₂CO₃), triethylamine) or organic complexing salts (Iron (III) citrate—FeCit), FeCl₃ and FePO₄).

In some embodiments, cross-linking agents are used in an amount of between 0.01 and 10 w/w % based on the weight of the adhesive, more preferably in an amount of between 0.1 and 5 w/w % based on the weight of the adhesive.

Adhesives may be applied to a support and cross-linked to the support. In some embodiments, cross-linking reactions are delayed until time of use e.g. by storing the device under conditions that inhibit cross-linking reactions. Various approaches are available to ensure stability of the devices and can include cold storage and transportation, addition of antioxidants, encapsulation of the cross-linking agents in temperature triggered materials, careful selection of cross-linking agents that do not react at common storage conditions or addition of cross-linking agents that require external energy to initiate the cross-linking reactions.

Suitable support materials include common biocompatible polymers including polyesters, polylactides, polypropylene, polyolefins, polyurethanes, polyamides, carbohydrate polymers and other natural or synthetic derived polymers.

In some embodiments, the adhesive may be used to adhere substances to blood or components thereof (plasma, red blood cells, white blood cells, and platelets or any combination thereof) as a result of the physical and/or chemical bonding interactions between the terminal adhesive group and blood or components thereof.

According to an embodiment, the adhesives described in the present disclosure may be used by adhering a first surface and a second surface by applying the adhesive to at least one of the first and second surfaces; and bringing at least a portion of the first and second surfaces into contact with each other. According to another embodiment, the adhesive of the present disclosure may be used by applying it neatly to one or both of the first and second surfaces. The first surface may comprise soft tissue and the second surface may comprise hard tissue such as bone. Alternatively, both surfaces may be soft tissue, or hard tissue such as bone. Alternatively, the first surface may comprise soft tissue and the second surface may be a surface of an implant or device. Alternatively, the first surface may comprise hard tissue such as bone and the second surface may be a surface of an implant or device.

According to an embodiment, the adhesive can be applied to the above surfaces using a source of external energy to enhance the curing of the adhesive with said surface.

In one embodiment, the adhesive itself may function as an implant such as where the adhesive may be rendered sufficiently rigid so as to permit it to be shaped for a particular medical purpose.

According to an embodiment, the adhesives described in the present disclosure may provide effective adhesion to one or more surfaces that are wet prior to application of the adhesive. The adhesive of the present disclosure may provide effective adhesion to one or more of the surfaces if submerged in aqueous media during application of the adhesive. The adhesive of the present disclosure may provide effective adhesion to one or more surfaces that are adhered together with the adhesive and wet following application of the adhesive. The adhesive of the present disclosure may continue to provide effective adhesion to one or more surfaces that are adhered together with the adhesive and submerged in aqueous media following application of the adhesive. The adhesive of the present disclosure may provide effective adhesion to one or more surfaces that are adhered together in the presence of blood. The adhesive of the present disclosure may continue to provide effective adhesion to one or more surfaces that are exposed to blood following bonding.

Non-limiting examples of soft-to-hard tissue binding include the attachment of tendons, muscles, cartilage or skin to bone.

Non-limiting examples of soft-soft tissue binding where the bioadhesive is advantageous include wound closure to curtail bleeding, closure of surgical incisions, skin grafts, cartilage attachment to skin, lung punctures, and cardiac tamponade.

Non-limiting examples of hard-to-hard tissue binding are described in US2015/0202046 incorporated herein by reference, and include bone fractures, bone grafts, bone waxes and bone void fillers.

Non-limiting examples of implantable devices that could benefit from attachment in situ using the bioadhesives include lead for real-time glucose monitoring meter, lead for a pacemaker, and insulin delivery system. More specifically, another example of an implantable device that could benefit from in situ attachment would be a flexible or ridged polymer with one side coated with adhesive for application in stabilization of bone fractures [33-34]. This could include an initially flexible structure that is rigidified and has a bioadhesive/cement located on one surface of the structure for sticking to bone.

According to an embodiment, the present disclosure also provides a device comprising a water insoluble adhesive having at least one compound of structure 1. The device comprises the water insoluble adhesive and a support, in one embodiment, a biocompatible support. The support may, for example, be a sheet structure and the water insoluble adhesive may be coated onto or impregnated into the sheet or portions thereof (e.g. there may be discrete bonding sites). In one embodiment, the sheet is a flexible rigidifiable biocompatible sheet i.e. a flexible sheet whose stiffness can be increased. In one embodiment, the water insoluble adhesive is located on a first surface of the sheet. In one embodiment, the sheet has first and second opposed surfaces and both surfaces are coated with the adhesive. In one embodiment, the biocompatible sheet is a sheet as described in US2015/0202046. In one embodiment, the main constituent on the biocompatible sheet structure is a biodegradable and/or bioresorbable polymer. In some embodiments, the polymer material contains repeating groups which include any one or a combination of amides, peptides, urethanes, esters, carbonates, anhydrides, ethers and sulphonamides. In one embodiment, the device further comprises a porous ceramic. In one embodiment, the device is a bone tape comprising a flexible rigidifiable biocompatible sheet as described in US2015/0202046 and a water insoluble bioadhesive as described herein. The dimensions of the sheet (length, width, thickness) may be varied depending on the application and the bone tape may be cut prior to use. The device may further comprise a removable protective sheet to protect the water insoluble adhesive adhesive prior to use. Preferred protective sheet materials include polyesters (specifically polycaprolactone), polylactides (PLA, PLGA, Polydioxanone, etc.), polycarbonates (specifically poly(trimethylene carbonate)) and other biocompatible polymers. The support material must have compatibility with the adhesive such that adhesion between the adhesive and support are sufficient to provide application specific performance over a relevant timeline (e.g. ˜6 weeks of strong bonding for bone healing). Incompatible support materials may be chemically or physically modified to improve adhesion by treatment with oxygen plasma, acid etchants, basic agents, binding agents or other suitable surface modifiers.

In one embodiment, the support is formed from polycaprolactone. which due to its mechanical properties and high similarities to the adhesive structure can result in good performance at physiological temperatures and strong bonding to the adhesive without pretreatment or modifications of the polycaprolactone surface. In one embodiment, polycaprolactone is used without pretreatment or modifications of the polycaporlactone surface.

The device may be an implant comprising a biocompatible support and a water insoluble adhesive as described herein coated onto or impregnated into the support.

The water insoluble adhesive and support components of the device may be hydrolysable or enzyme degradable under physiological conditions. Furthermore, the entire device may be hydrolysable or enzyme degradable under physiological conditions.

According to an embodiment, the adhesive of the present disclosure may be used to perform a number of functions, including but not limited to:

-   -   Align, orient, or fasten tissues together so they can heal     -   Align, orient, or fasten tissues together so that they are more         aesthetically desirable     -   Close a wound or void so fluid loss, pressure loss, air loss,         etc. is slowed or minimized     -   Seal a wound, defect or void by fixing another impermeable         material over the wound, defect or void     -   Affix a prosthetic or biomaterial     -   Localize a drug, drug delivery agent, sensor or other device in         a certain area.

In one embodiment, the water insoluble adhesive may be incorporated into or coated onto a patch or tape for use in medical procedures, such as craniomaxillofacial surgery.

According to an embodiment, the adhesive may be used for the fixation of medical devices to a target site or tissue. Examples may include fixation of a therapeutic patch, a surgical mesh for hernia, bone fractures, or other applications, an insulin delivery or monitoring device, a wound dressing or bandage, a sensor, a catheter, or a regenerative material such as a bio-scaffold.

According to an embodiment, the water insoluble adhesive may be used to render a biomedical mesh adherent to tissues. Examples may include a biomedical mesh that does not need to be sutured, screwed, stapled, or otherwise fastened to tissues or biological structures. Additional examples may include a biological mesh that provides improved fixation when compared to mechanical fixation alone. In a select embodiment, this could be used to adhere fragments of bone to a mesh, resulting in improved bone stabilization. In another embodiment, the adherent mesh may provide more uniform adhesion, improving healing. In another embodiment, the adherent mesh may integrate with cells better, improving integration with tissues. In another embodiment, the adherent mesh may be loaded with a drug, protein, biomaterial or other therapeutic agent to enhance or improve healing.

According to an embodiment, the water insoluble adhesive may be used to functionalize a surface of synthetic or natural biomaterials or devices. This may be used to improve cellular adhesion to the surface, control, select or recruit adhesion of preferential types of cells, or attach a therapeutic agent or compound to the surface to a synthetic or natural biomaterial or device. In a select embodiment, this could be used to adhere antibiotic or antifungal elements, rendering the surface less susceptible to bacterial or fungal contaminations. In another embodiment, a graft, stent or other biomaterial may be functionalized with antibodies or antifungals or growth factors using the described adhesives to facilitate adhesion such that desirable types of cells are preferentially recruited to the biomaterial. In another embodiment, the described adhesive may be used to functionalize a non-adherent surface so that cells or proteins are able to attach to the surface, enabling or improving surface functionalization and degree of integration, e.g. one surface of a support can be an adherent surface and the opposite surface can be a functionalized surface.

According to an embodiment, the adhesive may be dissolved or suspended in a solution where it is subsequently crosslinked in solution to form a a gel. This gel may encapsulate antibiotics, therapeutic or regenerative materials from the solution or may alternatively be impregnated with antibiotics, therapeutic or regenerative materials following formation.

According to an embodiment, the adhesive may be crosslinked in solution to form micro or nano sized particles, encapsulate antibiotics, therapeutic or regenerative materials from the solution or may alternatively be impregnated with antibiotics, therapeutic or regenerative materials following formation.

All documents referenced herein are incorporated by reference, however, it should be appreciated that any patent, publication, or other disclosure material, in whole or in part, that is incorporated by reference herein is incorporated only to the extent that the incorporated material does not conflict with definitions, statements, or other disclosure material set forth in this disclosure. As such, and to the extent necessary, the disclosure as explicitly set forth herein supersedes any conflicting material incorporated herein by reference.

The above description and accompanying drawings should be taken as illustrative of the invention and it is to be understood that it is intended to cover any variations, uses, or adaptations of the invention following, in general, the principles of the invention and including such departures from the present disclosure as come within known or customary practice within the art to which the invention pertains. The embodiments of the invention described above are intended to be exemplary only. The scope of the invention is therefore intended to be limited solely by the scope of the appended claims.

EXAMPLES

With the exception of Adhesive 6, which is prepared as a comparative control catechol-blocked non-adhesive system, all of the adhesives presented in the following examples present utility in different applications, with some adhesive examples presenting properties which make them better suited for certain applications compared to other adhesive examples. Particularly significant, the adhesive formulations as described herein may be used without solvent. This can be a significant advantage because, among other things, as demonstrated in Example 14, residual solvent can decrease the cohesive strength of adhesives.

Examples 1-8 present the syntheses of water insoluble adhesives of the present disclosure; example 9 demonstrates the biocompatibility of select adhesives, examples 10-12 present the adhesive properties of the adhesives of the present disclosure, example 13 presents a working example of a device comprising a water insoluble adhesives of the present disclosure, and example 14 presents the effect of residual solvent on the performance of adhesives disclosed herein.

Example 1: Difunctional PCL Adhesive (Adhesives 1a-b)

FIG. 17 shows a generalized reaction scheme for the synthesis of difunctional PCL adhesives in which the terminal hydroxyl groups of a PCL-diol reacts with one of two isocyanate groups of the diisocyanate molecule resulting in a-PCL-diisocyanate molecule. The free isocyanates then react with a reactive moiety (here an amine) present on the alkyl chain of the 4-alkylbenzene-1,2-diol derivative (here dopamine).

Example 1a: Synthesis of Adhesive 1a as an Example of a Difunctional PCL Adhesive a) Activation of the Dopamine Derivative (Dopa):

FIG. 18 shows the activation of dopamine hydrochloride. One molar equivalent of dopamine hydrochloride was dissolved in a minimum volume of anhydrous DMAc at room temperature. An equivalent molar amount of triethylamine was added to complex the hydrochloride salt from dopamine. This mixture was stirred for 30 minutes, yielding a cloudy solution. Triethylamine hydrochloride was separated from the activated dopamine by centrifuging for 10 minutes at 5000 rpm and −10° C. The activated dopamine was decanted from the solid triethylamine pellet and used immediately.

b) Synthesis of Isocyanate Terminated Polycaprolactone (PCL) Oligomers (Prepolymer 1a):

15 mmol of polycaprolactone diol with an average molecular weight of 530 g/mol (n=2) was added to a dry 250 mL 3-neck flask and degassed under vacuum at 60° C. for 12 h. The flask was purged with argon and 75 mL anhydrous DMAc was added through a septum with stirring under argon protection. Once the reaction mixture was completely clear, it was cooled to room temperature. 31.5 mmol of LDI (Methyl Ester L-Lysine Diisocyanate; 5% molar excess to the PCL hydroxyl groups) was added to the reaction mixture with a syringe through a silicone rubber septum and the mixture was stirred for 1 hour at room temperature. The reaction mixture was then ramped to 60° C. over 4 hours, followed by a second ramp to 75° C. over an additional 4 hours. Finally, the reaction was stirred at 75° C. for 2 hours, then cooled to room temperature to give the prepolymer 1 a.

c) Synthesis of PCL Based Oligomeric Dopamine Adhesive (Adhesive 1a):

Prepolymer 1a was functionalized by adding 33 mmol of activated dopamine in 60 mL of DMAc to the reaction mixture. An ice bath was used to dissipate heat from this rapid and exothermic step. The reaction was stirred for an additional 2 hours to ensure complete reaction, then the mixture was slowly poured into 500 mL ethyl acetate at room temperature. The mixture was slowly stirred for 30 minutes, then 250 mL deionized H₂O slightly acidified with a few drops of HCl was added. This two-phase system was transferred to a 1 L separatory funnel and washed 5 times with slightly acidic deionized water, retaining the organic phase between washings, to remove DMAc and undesirable reaction products. The solvent was removed under vacuum and the product was dissolved in a minimum volume of 1:1 acetone/ethanol. Approximately 5× the volume of hexanes was slowly added with stirring and the mixture was left in a fridge overnight. The cold solvent fraction was then decanted off, leaving the product stuck to the walls of the beaker.

Example 1b: Synthesis of Adhesive 1b as an Example of a Difunctional PCL Adhesive a) Activation of the Dopamine Derivative (Dopa):

Dopamine hydrochloride was activated as previously described. One molar equivalent of dopamine hydrochloride was dissolved into a minimum of anhydrous DMAc at room temperature. An equivalent amount of triethylamine was added to complex the hydrochloride salt from dopamine. The mixture was stirred for 30 minutes, yielding a cloudy solution. Triethylamine hydrochloride was separated from the activated dopamine by centrifuging for 10 minutes at 5000 rpm and −10° C. The activated dopamine was decanted from the solid triethylamine pellet and used immediately.

b) Synthesis of Isocyanate Terminated PCL Oligomers (Prepolymer 1b):

10 mmol of polycaprolactone diol with an average molecular weight of 2000 g/mol (n=28.5) was added to a dry 250 mL 3-neck flask and degassed under vacuum at 60° C. for 12 h. The flask was purged with argon and 50 mL anhydrous DMAc was added through a septum with stirring under argon protection. Once the reaction mixture was completely clear, it was cooled to room temperature. 21 mmol of LDI (Methyl Ester L-Lysine Diisocyanate, 5% molar excess to hydroxyl groups) was added to the reaction mixture with a syringe through a silicone rubber septum and the mixture was stirred for 1 hour at room temperature. The reaction mixture was then ramped to 60° C. over 4 hours, followed by a second ramp to 75° C. over an additional 4 hours. Finally, the reaction was stirred at 75° C. for 2 hours, then cooled to room temperature to give prepolymer 1 b.

c) Synthesis of PCL Based Oligomeric Dopamine Adhesive (Adhesive 1b):

Prepolymer 1 b was functionalized by adding 22 mmol of activated dopamine in 40 mL of DMAc to the reaction mixture. An ice bath was used to dissipate heat from this rapid and exothermic step. The reaction was stirred for an additional 2 hours to ensure complete reaction, then the mixture was slowly poured into 500 mL ethyl acetate at room temperature. The mixture was slowly stirred for 30 minutes, then 250 mL deionized H₂O slightly acidified with a few drops of HCl was added. This 2-phase system was transferred to a 1 L separatory funnel and washed 5 times with slightly acidic deionized water, retaining the organic phase between washings, to remove DMAc and undesirable reaction products. The solvent was removed under vacuum and the product was dissolved in a minimum volume of 1:1 acetone/ethanol. Approximately 5× the volume of hexanes was slowly added with stirring and the mixture was left in a fridge overnight. The cold solvent fraction was then decanted off, leaving the product stuck to the walls of the beaker.

Example 2: Trifunctional PCL Adhesive (Adhesives 2a-c)

FIG. 19 shows a generalized reaction scheme for the synthesis of trifunctional PCL adhesives in which the terminal hydroxyl groups of a PCL-triol reacts with one of two isocyanate groups of the diisocyanate molecule resulting in a PCL-triisocyanate molecule. The free isocyanates then react with a reactive moiety (here an amine) present on the alkyl chain of the 4-alkylbenzene-1,2-diol derivative (here dopamine)

Example 2a: Synthesis of Adhesive 2a as an Example of a Trifunctional PCL Adhesive a) Activation of the Dopamine Derivative (Dopa):

Dopamine hydrochloride was activated as previously described. One molar equivalent of dopamine hydrochloride was dissolved into a minimum of anhydrous DMAc at room temperature. An equivalent amount of triethylamine was added to complex the hydrochloride salt from dopamine. The mixture was stirred for 30 minutes, yielding a cloudy solution. Triethylamine hydrochloride was separated from the activated dopamine by centrifuging for 10 minutes at 5000 rpm and −10° C. The activated dopamine was decanted from the solid triethylamine pellet and used immediately.

b) Synthesis of Isocyanate Terminated PCL Oligomers (Prepolymer 2a):

Ten mmol of polycaprolactone triol with an average molecular weight of 300 g/mol (n=0.7) was added to a dry 250 mL 3-neck flask and degassed under vacuum at 60° C. for 12 h. The flask was purged with argon and 25 mL anhydrous DMAc was added through a septum with stirring under argon protection. Once the reaction mixture was completely clear, it was cooled to room temperature. 31.5 mmol of LDI (Methyl Ester L-Lysine Diisocyanate, 5% molar excess to hydroxyl groups) was added to the reaction mixture with a syringe through a silicone rubber septum and the mixture was stirred for 1 hour at room temperature. The reaction mixture was then ramped to 60° C. over 4 hours, followed by a second ramp to 75° C. over an additional 4 hours. Finally, the reaction was stirred at 75° C. for 2 hours, then cooled to room temperature to give prepolymer 2a.

c) Synthesis of PCL Based Oligomeric Dopamine Adhesive (Adhesive 2a)

Prepolymer 2a was functionalized by adding 33 mmol of activated dopamine in 50 mL of DMAc to the reaction mixture. An ice bath was used to dissipate heat from this rapid and exothermic step. The reaction was stirred for an additional 2 hours to ensure complete reaction, then the mixture was slowly poured into stirred deionized ice water (200 mL) at 0° C. Stirring was ceased, and Adhesive 2a was recovered as a thick viscous fluid on the bottom of the flask after decanting the water fraction. It was re-dissolved in acetone (75 mL) and precipitated out of solution with deionized water (200 mL) twice more to remove any residual triethylamine, dopamine, LDI derivatives and other reaction by-products.

Example 2b: Synthesis of Adhesive 2b as an Example of Trifunctional PCL Adhesive a) Activation of the Dopamine Derivative (Dopa):

Dopamine hydrochloride was activated as previously described. One molar equivalent of dopamine hydrochloride was dissolved into a minimum of anhydrous DMAc at room temperature. An equivalent amount of triethylamine was added to complex the hydrochloride salt from dopamine. The mixture was stirred for 30 minutes, yielding a cloudy solution. Triethylamine hydrochloride was separated from the activated dopamine by centrifuging for 10 minutes at 5000 rpm and −10° C. The activated dopamine was decanted from the solid triethylamine pellet and used immediately.

b) Synthesis of Isocyanate Terminated PCL Oligomers (Prepolymer 2b):

10 mmol of polycaprolactone triol with an average molecular weight of 900 g/mol (n=2.3) was added to a dry 250 mL 3-neck flask and degassed under vacuum at 60° C. for 12 h. The flask was purged with argon and 25 mL anhydrous DMAc was added through a septum with stirring under argon protection. Once the reaction mixture was completely clear, it was cooled to room temperature. 31.5 mmol of LDI (Methyl Ester L-Lysine Diisocyanate, 5% molar excess to hydroxyl groups) was added to the reaction mixture with a syringe through a silicone rubber septum and the mixture was stirred for 1 hour at room temperature. The reaction mixture was then ramped to 60° C. over 4 hours, followed by a second ramp to 75° C. over an additional 4 hours. Finally, the reaction was stirred at 75° C. for 2 hours, then cooled to room temperature to give prepolymer 2b.

c) Synthesis of PCL Based Oligomeric Dopamine Adhesive (Adhesive 2b)

Prepolymer 2b was functionalized by adding 33 mmol of activated dopamine in 50 mL of DMAc to the reaction mixture. An ice bath was used to dissipate heat from this rapid and exothermic step. The reaction was stirred for an additional 2 hours to ensure complete reaction, then the mixture was slowly poured into stirred deionized water (200 mL) at room temperature. Stirring was ceased, and Adhesive 2b was recovered as a thick viscous fluid on the bottom of the flask after decanting the water fraction. It was re-dissolved in acetone (75 mL) and precipitated out of solution with deionized water (200 mL) twice more to remove any residual triethylamine, dopamine, LDI derivatives and other reaction by-products.

Example 2c: Synthesis of Adhesive 2c as an Example of Trifunctional PCL Adhesive a) Activation of the Dopamine Derivative (Dopa):

Dopamine hydrochloride was activated as previously described. One molar equivalent of dopamine hydrochloride was dissolved into a minimum of anhydrous DMAc at room temperature. An equivalent amount of triethylamine was added to complex the hydrochloride salt from dopamine. The mixture was stirred for 30 minutes, yielding a cloudy solution. Triethylamine hydrochloride was separated from the activated dopamine by centrifuging for 10 minutes at 5000 rpm and −10° C. The activated dopamine was decanted from the solid triethylamine pellet and used immediately.

b) Synthesis of Isocyanate Terminated PCL Oligomers (Prepolymer 2c):

10 mmol of polycaprolactone triol with an average molecular weight of 2000 g/mol (n=5.5) was added to a dry 250 mL 3-neck flask and degassed under vacuum at 60° C. for 12 h. The flask was purged with argon and 50 mL anhydrous DMAc was added through a septum with stirring under argon protection. Once the reaction mixture was completely clear, it was cooled to room temperature. 31.5 mmol of LDI (Methyl Ester L-Lysine Diisocyanate, 5% molar excess to hydroxyl groups) was added to the reaction mixture with a syringe through a silicone rubber septum and the mixture was stirred for 1 hour at room temperature. The reaction mixture was then ramped to 60° C. over 4 hours, followed by a second ramp to 75° C. over an additional 4 hours. Finally, the reaction was stirred at 75° C. for 2 hours, then cooled to room temperature to give prepolymer 2c.

c) Synthesis of PCL Based Oligomeric Dopamine Adhesive (Adhesive 2c)

Prepolymer 2c was functionalized by adding 33 mmol of activated dopamine in 50 mL of DMAc to the reaction mixture. An ice bath was used to dissipate heat from this rapid and exothermic step. The reaction was stirred for an additional 2 hours to ensure complete reaction, then the mixture was slowly poured into stirred deionized water (200 mL) at room temperature. Stirring was ceased, and Adhesive 2c was recovered as a thick viscous fluid on the bottom of the flask after decanting the water fraction. It was re-dissolved in a 1:1 ethanol/acetone mixture (150 mL) and precipitated out of solution with slightly acidified deionized water (500 mL) twice more to remove any residual reaction by-products

Example 3: Tetrafunctional PCL Adhesive (Adhesive 3)

FIG. 20 shows a generalized reaction scheme for the synthesis of tetrafunctional PCL adhesives in which the terminal hydroxyl groups of a PCL-tetraol reacts with one of two isocyanate groups of the diisocyanate molecule resulting in a PCL-Tetraisocyanate molecule. The free isocyanates then react with a reactive moiety (here an amine) present on the alkyl chain of the 4-alkylbenzene-1,2-diol derivative (here dopamine).

Example 3a: Synthesis of Adhesive 3a as an Example of Tetrafunctional PCL Adhesive a) Activation of the Dopamine Derivative (Dopa):

Dopamine hydrochloride was activated as previously described. One molar equivalent of dopamine hydrochloride was dissolved into a minimum of anhydrous DMAc at room temperature. An equivalent amount of triethylamine was added to complex the hydrochloride salt from dopamine. The mixture was stirred for 30 minutes, yielding a cloudy solution. Triethylamine hydrochloride was separated from the activated dopamine by centrifuging for 10 minutes at 5000 rpm and −10° C. The activated dopamine was decanted from the solid triethylamine pellet and used immediately.

b) Synthesis of Isocyanate Terminated PCL Oligomers (Prepolymer 3a):

10 mmol of polycaprolactone tetrol with an average molecular weight of 1000 g/mol (n=2) was added to a dry 250 ml 3-neck flask and degassed under vacuum at 60° C. for 12 h. The flask was purged with argon and 50 mL anhydrous DMAc was added through a septum with stirring under argon protection. Once the reaction mixture was completely clear, it was cooled to room temperature. 42 mmol of LDI (5% molar excess to hydroxyl groups) was added to the reaction mixture with a syringe through a silicone rubber septum and the mixture was stirred for 1 hour at room temperature. The reaction mixture was then ramped to 60° C. over 4 hours, followed by a second ramp to 75° C. over an additional 4 hours. Finally, the reaction was stirred at 75° C. for 2 hours, then cooled to room temperature to give Prepolymer 3a.

c) Synthesis of PCL Based Oligomeric Dopamine Adhesive (Adhesive 3a)

Prepolymer 3a was functionalized by adding 44 mmol of activated dopamine in 50 mL of DMAc to the reaction mixture. An ice bath was used to dissipate heat from this rapid and exothermic step. The reaction was stirred for an additional 2 hours to ensure complete reaction, then the mixture was slowly poured into a mixture of diethyl ether (700 mL) and deionized water (300 mL) at room temperature. The mixture was stirred vigorously for 2 hours, then stirring was ceased and the reaction mixture was cooled in the fridge. The liquid phase was decanted off, and Adhesive 3a was recovered from the walls of the beaker. It was re-dissolved in a mixture of acetone/ethyl acetate (200 mL) and precipitated out of solution with hexanes (500 mL) to remove any residual reaction by-products.

Example 4: Pentafunctional PCL Adhesive (Adhesive 4)

FIG. 21 shows a generalized reaction scheme for the synthesis of pentafunctional PCL adhesive in which the terminal hydroxyl groups of a PCL-Pentaiol reacts with one of two isocyanate groups of the diisocyanate molecule resulting in a PCL-Pentaisocyanate molecule. The free isocyanates then react with a reactive moiety (here an amine) present on the alkyl chain of the 4-alkylbenzene-1,2-diol derivative (here dopamine) to give Adhesive 4.

Example 5: Hexafunctional PCL Adhesive (Adhesive 5)

FIG. 22 shows a generalized reaction scheme for the synthesis of hexafunctional PCL adhesive in which the terminal hydroxyl groups of a PCL-Hexol reacts with one of two isocyanate groups of the diisocyanate molecule resulting in a PCL-Triisocyanate molecule. The free isocyanates then react with a reactive moiety (here an amine) present on the alkyl chain of the 4-alkylbenzene-1,2-diol derivative (here dopamine) to give Adhesive 5.

Example 6: Trifunctional PCL Control (Adhesive 6)

For comparative purposes, Adhesive 6 was prepared as a negative control from a dopamine derivative in which the catechol groups were blocked by methoxy functional groups.

a) Synthesis of Isocyanate Terminated PCL Oligomers (Prepolymer 6)

10 mmol of polycaprolactone triol with an average molecular weight of 900 g/mol (n=2.3) was added to a dry 250 mL 3-neck flask and degassed under vacuum at 60° C. for 12 h. The flask was purged with argon and 25 mL anhydrous DMAc was added through a septum with stirring under argon protection. Once the reaction mixture was completely clear, it was cooled to room temperature. 31.5 mmol of LDI (Methyl Ester L-Lysine Diisocyanate, 5% molar excess to hydroxyl groups) was added to the reaction mixture with a syringe through a silicone rubber septum and the mixture was stirred for 1 hour at room temperature. The reaction mixture was then ramped to 60° C. over 4 hours, followed by a second ramp to 75° C. over an additional 4 hours. Finally, the reaction was stirred at 75° C. for 2 hours, then cooled to room temperature to give prepolymer 6.

b) Synthesis of PCL Based Oligomeric Dopamine Control (Adhesive 6)

Prepolymer 6 was functionalized with methoxy capped dopamine by adding 33 mmol of 3,4-Dimethoxyphenethylamine in 50 mL of DMAc to the reaction mixture. An ice bath was used to dissipate heat from this rapid and exothermic step. The reaction was stirred for an additional 2 hours to ensure complete reaction, then the mixture was slowly poured into stirred deionized water (200 mL) at room temperature. Stirring was ceased, and Adhesive 6 was recovered as a thick viscous fluid on the bottom of the flask after decanting the water fraction. It was re-dissolved in acetone (100 mL) and precipitated out of solution with deionized water (200 mL) twice more to remove any residual reaction by-products.

Example 7: Difunctional Poly(dimethylsiloxane) (PDMS) Adhesive (Adhesive 7)

FIG. 23 shows a generalized reaction scheme for the synthesis of for the synthesis of difunctional PDMS adhesive in which the terminal hydroxyl groups of a PDMS-Diamine reacts with one of two isocyanate groups of the diisocyanate molecule resulting in a PDMS-Diisocyanate molecule. The free isocyanates then react with a reactive moiety (here an amine) present on the alkyl chain of the 4-alkylbenzene-1,2-diol derivative (here dopamine).

Example 7a: Synthesis of Adhesive 7a as an Example of Difunctional PDMS Adhesive a) Activation of the Dopamine Derivative (Dopa):

Dopamine hydrochloride was activated as previously described. One molar equivalent of dopamine hydrochloride was dissolved into a minimum of anhydrous DMAc at room temperature. An equivalent amount of triethylamine was added to complex the hydrochloride salt from dopamine. The mixture was stirred for 30 minutes, yielding a cloudy solution. Triethylamine hydrochloride was separated from the activated dopamine by centrifuging for 10 minutes at 5000 rpm and −10° C. The activated dopamine was decanted from the solid triethylamine pellet and used immediately.

b) Synthesis of Isocyanate Terminated PDMS Oligomers (Prepolymer 7a):

10.5 g of diamine terminated PDMS with an average molecular weight of 2500 g/mol (n=32) was added to a dry 250 mL 3-neck flask and degassed under vacuum at 60° C. for 12 h. The flask was purged with argon and 100 ml anhydrous DMAc was added through a septum with stirring under argon protection. Once the reaction mixture was completely clear, it was cooled in an ice bath. 1.87 g of LDI (5% molar excess to amine groups) was added to the reaction mixture with a syringe through a silicone rubber septum. The reaction mixture was stirred in the ice bath for 2 hours, and then an additional 2 hours at room temperature to give prepolymer 7a.

c) Synthesis of PDMS Based Oligomeric Dopamine Adhesive (Adhesive 7a)

Prepolymer 7a was functionalized by adding 1.76 g activated dopamine in 40 mL of DMAc to the reaction mixture. An ice bath was used to dissipate heat from this rapid and exothermic step. The reaction was stirred for an additional 2 hours to ensure complete reaction, then the mixture was slowly poured into methanol (300 mL) at room temperature. The mixture was stirred vigorously for 1 hour, then stirring was ceased and the reaction mixture was cooled in the fridge. The liquid phase was decanted off, and the Adhesive 7a was recovered from the walls of the beaker. It was re-dissolved in acetone (200 mL) and precipitated by pouring into methanol a second time (500 mL) to remove any residual reaction by-products.

Example 8: Difunctional Poly(Hexamethylene Carbonate) (PCN) Adhesive (Adhesive 8)

FIG. 25 shows a generalized reaction scheme for the synthesis of difunctional PCN adhesives in which the terminal hydroxyl groups of a PCN-Diol reacts with one of two isocyanate groups of the diisocyanate molecule resulting in a PCN— Diisocyanate molecule. The free isocyanates then react with a reactive moiety (here an amine) present on the alkyl chain of the 4-alkylbenzene-1,2-diol derivative (here dopamine).

Example 8a: Synthesis of Adhesive 8a as an Example of Difunctional PCN Adhesive a) Activation of the Dopamine Derivative (Dopa):

Dopamine hydrochloride was activated as previously described. One molar equivalent of dopamine hydrochloride was dissolved into a minimum of anhydrous DMAc at room temperature. An equivalent amount of triethylamine was added to complex the hydrochloride salt from dopamine. The mixture was stirred for 30 minutes, yielding a cloudy solution. Triethylamine hydrochloride was separated from the activated dopamine by centrifuging for 10 minutes at 5000 rpm and −10° C. The activated dopamine was decanted from the solid triethylamine pellet and used immediately.

b) Synthesis of Isocyanate Terminated PCN Oligomers (Prepolymer 8a):

12.6 g of dialcohol terminated Poly(hexamethylene carbonate) diol (PCN) with an average molecular weight of 1048 g/mol (n=7) was added to a dry 250 mL 3-neck flask and degassed under vacuum at 60° C. for 12 h. The flask was purged with argon and 50 mL anhydrous DMAc was added through a septum with stirring under argon protection. Once the reaction mixture was completely clear, it was cooled to room temperature. 5.3 g of LDI (5% molar excess to alcohol groups) was added to the reaction mixture with a syringe through a silicone rubber septum. The reaction mixture was then ramped to 60° C. over 4 hours, followed by a second ramp to 75° C. over an additional 4 hours. Finally, the reaction was stirred at 75° C. for 2 hours, then cooled to room temperature to give prepolymer 8a.

c) Synthesis of PCN Based Oligomeric Dopamine Adhesive (Adhesive 8a)

Prepolymer 8a was functionalized by adding 5.0 g activated dopamine in 100 mL of DMAc to the reaction mixture. An ice bath was used to dissipate heat from this rapid and exothermic step. The reaction was stirred for an additional 2 hours to ensure complete reaction, then the mixture was slowly poured into a 1:1 mixture of hexanes and diethyl ether (500 mL) at room temperature. The mixture was stirred vigorously for 1 hour, then stirring was ceased and the reaction mixture was cooled in the fridge. The liquid phase was decanted off, and Adhesive 8a was recovered from the walls of the beaker. It was re-dissolved in acetone (250 mL) and precipitated by pouring into cold methanol (500 mL) to remove any residual reaction by-products.

Example 9: Cytotoxicity Testing

Cytotoxicity Assays: In vitro cytotoxicity of adhesive formulations was assessed by direct contact with cells, according to ISO 10993-5 [35], which describes test methods to evaluate in vitro cytotoxicity of medical devices and, therefore, determine the in vitro biological response of mammalian cells using appropriate parameters. DNA mass quantification and Water-soluble tetrazolium (WST-1) assays were used to evaluate the toxicity of the formulations to a cell line. Negative and positive controls consisted of growth media with untreated cells and 5% Dimethyl sulfoxide (DMSO), respectively.

Cell Culture and Sample Preparation: A10 smooth muscle cell line (ATCC, CRL-1476™) were cultured in Dulbecco's modified Eagle's medium (DMEM), supplemented with 100 U mL⁻¹ penicillin/100 μg of streptomycin and 10% fetal bovine serum in a humidified atmosphere at 37° C. with 5% CO₂. The medium was changed every other day, allowing the cells to grow and reach confluency. When the cells reached 80-90% confluence, they were passaged following treatment with 0.25% trypsin-EDTA solution. This procedure was repeated until the cells entered their standard cellular cycle [36, 37]. Samples of adhesives were pre-conditioned in an incubator with DMEM for 24 h. Then, cells were seeded onto the samples, to which 200 μL of A10 suspension (approximately 25,000 cells/mL) was added. The seeded specimens were confined in the wells of a 96-well plate for 24 h, 72 h and 7 days.

DNA mass quantification: At each time-point, cells were lysed with ice-cold lysis buffer (0.05% Triton X-100, 50 mM EDTA in PBS) for 1 h and tested for DNA assay as previously described [37-39]. First, 0.1% Hoechst Dye 33258 was diluted in a Trizma base/NaCl/EDTA buffer (0.10 M Trizma base, 0.2 M NaCl and 0.001 M EDTA in dH2O, pH 7.4) and 100 μL was added to a 96-well plate (Microfluor 2 Black, VWR). Then, 10 μL of cell lysate was added to the dye and read against a calf thymus DNA standard in a fluorescence microplate reader (BioTek Cytation 3, Biotek, Winooski, Vt., USA), with the excitation wavelength set at 360 nm and the emission wavelength observed at 460 nm [36].

WST-1 assay: For the WST assay, after removing media and rinsing with 1× with PBS, 200 μL of DMEM was added to each well. Next, 20 μL of the WST reagent was added to each well and the microplate will be incubated at 37° C. with 5% CO₂ for 1 h. The absorbance was read using a multi-mode reader (BioTek Cytation 3, Biotek, Winooski, Vt., USA) at 450 nm, with a reference wavelength of 650 nm [36]. Cell viability (%) was obtained using the equation:

${{Cell}{{viability}{}(\%)}} = {\left\lbrack {1 - \left\{ \frac{{At} - {Ab}}{{At} - {Ac}} \right\}} \right\rbrack \times {{100\left\lbrack {40} \right\rbrack}.}}$

Statistical analysis: Data was analyzed using the software PASW Statistics 21.0 (SPSS Inc, Chicago, Ill., USA). Two-Way analysis of variance (ANOVA) and Tukey's multiple comparison post-hoc tests will be used to determine a statistical significance between the groups for the DNA mass quantification and WST-1 assays. Homogeneity of variance and normality were verified with Levene's and Shapiro-Wilk tests, respectively. The confidence interval for all the tests will be set at 95%.

TABLE 1 DNA assay results for A10 cells exposed to select adhesives after 24 h, 72 h and 7 days incubation at 37° C. with 5% CO₂. Cell viability results are relative to values for DMEM negative control at each time point. 5% DMSO was used as a positive control. Results are expressed as Mean ± Standard Deviation, n = 4. Relative DNA mass (%) Group 24 h 72 h 7 d DMEM (Negative control) 100.0 ± 9.2  100.0 ± 12.1 100.0 ± 21.1 5% DMSO (Positive control) 15.3 ± 5.3  1.3 ± 1.9  1.4 ± 1.6 Adhesive 2b 102.6 ± 16.2 87.0 ± 6.0 89.2 ± 7.2 Adhesive 2c 104.3 ± 10.5  95.6 ± 10.1 88.3 ± 8.9 Adhesive 5 128.8 ± 13.0 109.9 ± 28.2 71.9 ± 5.5 Adhesive 3a  74.7 ± 18.2 36.5 ± 7.2  48.8 ± 18.5

TABLE 2 WST-1 cell viability assay results for A10 cells exposed to select adhesives after 24 h, 72 h and 7 days incubation at 37° C. with 5% CO₂. Cell viability results are relative to values for DMEM negative control at each time point. 5% DMSO was used as a positive control. Results are expressed as Mean ± Standard Deviation, n = 4. Relative Cell viability (%) Group 24 h 72 h 7 d DMEM (Negative control) 100.0 ± 6.5  100.0 ± 5.8  100.0 ± 12.3  5% DMSO (Positive control) 18.4 ± 0.9  4.4 ± 1.1 1.0 ± 0.5 Adhesive 2b 77.1 ± 2.4  79.7 ± 10.0 74.0 ± 10.0 Adhesive 2c 69.3 ± 9.1 75.5 ± 4.2 77.4 ± 16.2 Adhesive 5 83.5 ± 2.4 70.6 ± 8.0 74.5 ± 24.3 Adhesive 3a 100.2 ± 13.4 56.9 ± 3.9 60.5 ± 8.3 

Tables 1 and 2 show that many of the adhesive systems exhibit cytocompatibility 70%) after at least 24 hrs of contact with the A10 cell lines, indicating their suitability for use in medical device applications.

Example 10: Determination of the Thermal Properties of a Bioadhesive

Melting and glass transition data was obtained by modulated differential scanning calorimetry (mDSC). calorimetry studies were performed on a DSC Q200 (TA Instruments, Newcastle, Del., U.S.A.) equipped with a RCS90 refrigerated cooling system. Each sample (4-8 mg) was hermetically sealed into an aluminium DSC pan, and subsequently introduced into the DSC sample chamber continuously which was purged with a dry nitrogen flow of 60 m L/m in. The sample was equilibrated at 100° C. for 2 minutes to erase thermal history and/or facilitate crosslinking in the presence of crosslinking agents. A modulation frequency with an amplitude of 1.0° C./minute was initiated, and the sample was then cooled at a rate of 10.0° C./min down to −80° C. where it was held isothermally for 2 min. Finally, the sample was heated from −80° C. to 100° C. at a rate of 10.0° C./min and held isothermally for an additional 2 minutes. Thermal properties were calculated from the thermograms with TA Universal Analysis 2000 software.

TABLE 3a Glass transition temperature (Tg) of non-crosslinked adhesives and mixtures as determined by DSC from the midpoint of the Tg transition curve on the heating cycle. Samples were run in hermetically sealed aluminium DSC pans with 3-6 mg of sample per run. Tg values determined by the TA Universal Analysis 2000 software from samples run at 10° C./min with a continuous modulation at an amplitude of 1.0° C./minute. Comparison between heat flow, reversable heat flow, and non-reversable heat flow thermograms were used to isolate the glass transition events based on their second order phase transition behaviour. Adhesive Glass Transition Temperature-Tg (° C.) Adhesive 1b −51.7 ± 2.3  Adhesive 2a −1.2 ± 1.0 Adhesive 2b −21.5 ± 1.8  Adhesive 2c −40.8 ± 1.5  Adhesive 3a −8.1 ± 1.4 Adhesive 5 14.2 ± 3.0 Adhesive 7a −18.2 ± 10.3 Adhesive 8a −32.0 ± 4.7  Mixture (wt/wt %) 60% Adhesive 5a +  0.7 ± 2.3 40% Adhesive 2b Mixture (wt/wt %) 70 Adhesive 5a +  6.6 ± 2.0 30% Adhesive 2b Mixture (wt/wt %) 80% Adhesive 5a + 11.9 ± 0.6 20% Adhesive 2b Mixture (wt/wt %) 90% Adhesive 5a + 18.0 ± 0.3 10% Adhesive 2b

TABLE 3b Glass transition temperature (Tg) of crosslinked adhesives as determined by DSC from the midpoint of the Tg transition curve on the heating cycle. Crosslinked samples were obtained upon handmixing of the crosslinking agent with the adhesive at room temperature at the desired weight ratios immediately prior to sample pan preparation. Samples were run in hermetically sealed aluminium DSC pans with 3-6 mg of sample per run. Tg values were determined by the TA Universal Analysis 2000 software from samples run at 10° C./min with a continuous modulation at an amplitude of 1.0° C./minute. Comparison between heat flow, reversable heat flow, and non-reversable heat flow thermograms were used to isolate the glass transition events based on their second order phase transition behaviour. Adhesive Glass Transition Temperature-Tg (° C.) Adhesive 2a + 5% wt/wt FeCl₃  49.5 ± 10.4 Adhesive 2a + 5% wt/wt FePO₄ 49.0 ± 1.2 Adhesive 2a + 5% wt/wt FeCit 47.4.0 ± 2.1   Adhesive 2a + 5% wt/wt Na₃VO₄ 53.4 ± 2.0 Adhesive 2a + 5% wt/wt Na₂CO₃ 48.2 ± 0.8 Adhesive 2a + 5% wt/wt TBAP 53.8 ± 2.3 Adhesive 2b + 5% wt/wt FePO₄ −10.8 ± 0.6  Adhesive 2b + 5% wt/wt TBAP −11.6 ± 0.8  Adhesive 5 + 5% wt/wt TBAP 22.0 ± 0.9

Differential scanning calorimetry was used to determine the transition temperatures of the bioadhesives described herein. None of the adhesives displayed sharp or well-defined melting points; instead they all possessed well defined and narrow glass transition temperatures. These indicated the absence of crystalline domains and the inherent nature of their amorphous state, respectively. Higher glass transition temperatures are typical of glassy materials, whilst materials with lower glass transition temperatures remain amorphous for longer/until lower temperatures.

Variations in the glass transition temperatures of the non-crosslinked adhesives (Table 3a) were observed related to the inherent glass transition temperatures of the oligomeric backbone chemistry and were also related to oligomer length and catechol functionalization degree.

Adhesive mixtures which were physically blended (i.e., not chemically crosslinked; Table 3a) generally displayed only a single glass transition temperature between the range of the two mixtures, indicating complete solubilization of the adhesives with each other upon mixing. Typically, the resulting glass transition temperature was more heavily weighted towards the major weight constituent of the mixture, as can be seen from the changes in the mixing ratio between Adhesive 5a and Adhesive 2b in Table 3a.

Table 3b, on the other hand, shows that upon heating the adhesives in the presence of the crosslinking agents, the glass transitions shifted to notably higher temperatures, indicative of the successful rigidification of the low molecular weight—insoluble adhesives described herein. Importantly, Table 3b shows that similar degrees of rigidification could be obtained with the use of facile non-toxic crosslinking agents such as iron (III) phosphate, which is widely used in nutritional supplements for humans, as compared to more toxic crosslinkers such as the periodate (TBAP) or caustic iron (III) chloride.

However, while Table 3b shows a relative insensitivity of the adhesives to the nature of the crosslinking agent, it does reveal that the different adhesives do not respond to crosslinking-mediated rigidification in the same manner. For example, upon crosslinking, Adhesive 2a undergoes a change in Tg of −50° C., whilst Adhesive 2b and Adhesive 5 undergo a substantially smaller increase in Tg of −10° C. each. Consideration of the catechol group densities of the different adhesives does not readily explain this difference in the rigidification of the adhesives; both Adhesives 2a and 5 possess similar catechol group densities per unit mass of adhesive (2 mmol/g) whilst the catechol density of Adhesive 2b is 1.5 mmol/g. On the other hand, the steric complexities of the adhesives—which affect and eventually limit the interactions of the adhesive moieties with the crosslinkers—do increase with their molecular masses, indicating that the lower molecular weight systems are more amenable to rigidification upon crosslinking compared to larger molecular weight systems (MW of adhesives 2a, 2b and 5 are 1401, 2018 and 3019, respectively). Thus, with careful tuning based on informed structure-property correlations, it is possible to identify and select specific adhesive-only and/or adhesive-adhesive combinations that, when crosslinked, would present a range of tunable material properties such as the desired degree of rigidity, setting rate, and/or different degrees of hardness and/or flexibility.

Example 11: Testing Adhesion on Different Interfaces

This section presents evidence that the adhesives are functional with a variety of adherends, and, therefore, their utility for a wide range of medical device applications.

Example 11 a: Skin/Glass

Porcine skin was fixed to a dry glass microscopy slide using Adhesive 2a adhesive. 100 mg of adhesive was spread evenly on a warmed glass slide and a strip (3.0 cm×10.0 cm×1.0 cm) of porcine skin freshly obtained from a local butcher was pressed by hand force onto the slide with the skin side in contact with the adhesive coated side of the glass slide for approximately 5 seconds. A 100 g brass weight was then sutured through the tissue and hung from the skin so that the weight of the tissue and brass weight was loaded entirely onto the biocompatible adhesive glass/skin bond. The adherend samples were left loaded and undisturbed at room temperature (approximately 22° C.). Photographs were taken 10 minutes after the weight was initially loaded (FIG. 26 ). Photo depicts a 100 g weight connected to porcine skin after hanging suspended by the skin/adhesive/polymer bond at room temperature for 10 minutes.

Example 11b: Bone/Bone

Porcine rib bones were bound together using Adhesive 2a adhesive. 50 mg of the adhesive was spread evenly on a 37° C. rib bone, that was previously immersed in a sterile saline solution (0.9% NaCl) at 37° C. for 1 hour and blotted with cotton gauze to remove excess saline just prior to adhesive application. A second porcine rib subjected to identical conditions was pressed by hand force firmly onto the first such that the area with the adhesive made contact with both ribs for approximately 5 seconds. A 100 g brass weight was tied around the lower rib and freely hung so that the weight of the bone and brass weight was held by the biocompatible adhesive bone/bone bond. The adherend samples were left loaded and undisturbed at room temperature (approximately 22° C.). Photographs were taken 10 minutes after the weight was initially loaded (FIG. 27 ). Photo depicts a 100 g weight connected to two porcine rib bones bound together by a bone/adhesive/bone bond after hanging suspended at room temperature for 10 minutes.

Example 11c: Bone/Skin

Porcine rib and skin were bound together using Adhesive 2a adhesive. 50 mg of the adhesive was spread evenly on a warmed (−37° C.) rib bone and a piece of skin at room temperature was stuck to the rib. A suture was placed through the skin to secure it and allow it to hang freely. No load was applied, and photographs were taken immediately after the tissue samples were bound together (FIG. 28 ). Photo depicts a porcine rib bone bound to porcine skin by a bone/adhesive/skin bond after hanging suspended at room temperature for 10 minutes.

Example 11d: Skin/Skin

Porcine fatty skin tissues were bound together using Adhesive 2a adhesive. 50 mg of the adhesive was spread evenly onto a warmed (−37° C.) piece of skin tissue and a second piece of tissue was pressed onto the first for approximately 5 seconds. No load was applied, and photographs were taken immediately after the tissue samples were bound together. Photographs were taken immediately after the tissue samples were bound together (FIG. 29 ). Photo depicts porcine skin bound to porcine skin by a skin/adhesive/skin bond immediately after application at room temperature.

Example 11e: Bone/Polymer/Skin

A 2.0 cm×6.0 cm×0.4 mm piece of polycaprolactone (Mw=90 000 g/mol) was coated evenly on one side with 50 mg Adhesive 2b. One end of the tape was bound to the porcine rib bone and the other end of the polycaprolactone tape was bound to porcine skin. An even layer of 50 mg of Adhesive 2b was present at each interface between the polycaprolactone and the tissues. The bone and tissue specimens were affixed to the polycaprolactone by being briefly pinched (approximately 5 seconds for each interface) so that they overlapped with the adhesive coated area. The porcine bone was clamped to a retort stand so that the polycaprolactone and porcine skin was suspended hanging freely from the bone. A 100 g brass weight was fixed to the porcine skin with a suture and hung freely to load the test sample. The brass weight and testing specimens were fully supported by the Adhesive 2b adhesive at both the skin to polycaprolactone and bone to polycaprolactone interfaces. The adherend samples were left loaded and undisturbed at room temperature (approximately 22° C.). Photographs were taken 10 minutes after the weight was initially loaded (FIG. 30 ). This is an example of a soft tissue/device and device/hard tissue interfaces. Photo depicts a polymeric film bound at the top to a porcine rib bone and bound at the bottom to a piece of porcine skin. A 100 g weight is suspected such that the loading is simultaneously on both the polymer/adhesive/bone and polymer/adhesive/skin bond, and the photo was captured after hanging suspended at room temperature for 10 minutes.

Example 12: Testing Adhesion Strength

Adhesion strength is a major design criterion for any adhesive. Here we define adhesion strength in shear, in either compression or tension depending on the sample type. Adhesion strength values were obtained from the maximum stress (converted to Pa from the applied force and cross-sectional area in contact between the two substrates tested). Adhesion was tested using a variety of temperatures, substrates, and formulations with and without induced crosslinking.

In general, adhesives with higher crosslinking density, higher melting temperatures and/or higher Tg values were less elastic, with little or no plastic deformation and a catastrophic failure mechanism. Without wishing to be bound by a theory, this is typical of materials with reduced elasticity and reflective of elevated crosslinking and/or being tested in a rigid or glassy state where there is limited plastic deformation of the adhesive oligomers, thus limiting rearrangement and elastic deformation or strain hardening. The less rigid adhesives generally failed by a ductile failure mode following a degree of plastic deformation.

Example 12a: The Effect of Crosslinkers and Substrates

To determine the effect of different crosslinkers on adhesion strength, several oxidants and complexing agents were mixed into adhesives at different weight ratios and applied to samples and allowed to cure. Adhesion strength was measured using a compressive shear test.

Crosslinking agents in this test included the inorganic oxidants Na₃VO₄ and tetrabutylammonium (meta)periodate (TBAP), an inorganic base (Na₂CO₃), an organic complexing salt (iron (III) citrate—FeCit), and two inorganic complexing salts (FeCl₃ and FePO₄). Briefly, crosslinkers were hand mixed into different adhesives on glass slides with the aid of heat and immediately applied onto aluminum, ceramic or glass substrates using a contact area of 90 mm². Samples were loaded in shear on an Instron 4301 universal testing machine under modified ASTM D905-08 conditions.

TABLE 4a Adhesion properties of bioadhesives using varying crosslinking agents and concentrations. Testing was conducted on an Instron 4301 universal testing machine with a 1000 N load cell and an applied strain rate of 2 mm/min at ambient room temperature on standard sized samples consisting of two pieces of dry aluminium or ceramic or glass adherends with approximately 0.20 g of adhesive between surfaces. Contact surface areas were kept nearly constant (~90 mm²) for all samples in the set. Results are expressed as Mean ± standard deviation, n = 4. Glass is defined as commercially available plain glass slides. Ceramic samples are composed of calcium polyphosphate tablets. Adhesive, Crosslinking agent, Substrate Adhesive Strength (MPa) Adhesive 2a + 5% wt/wt Na₃VO₄ (Aluminium) 2.7 ± 0.9 Adhesive 2a + 2.5% wt/wt Na₃VO₄ (Aluminium) 6.2 ± 1.9 Adhesive 2a + 5% wt/wt Na₂CO₃ (Aluminium) 3.0 ± 0.9 Adhesive 2a + 2.5% wt/wt Na₂CO₃ (Aluminium) 5.8 ± 2.8 Adhesive 2a + 5% wt/wt Na₃VO₄ (Ceramic) 1.2 ± 0.6 Adhesive 2a + 5% wt/wt Na₂CO₃ (Glass) 1.4 ± 0.5 Adhesive 2a + 5% wt/wt TBAP (Aluminium) 8.2 ± 2.7 Adhesive 2a + 2.5% wt/wt TBAP (Aluminium) 8.4 ± 2.2 Adhesive 2a + 5% wt/wt FeCl₃ (Aluminium) 1.7 ± 0.5 Adhesive 2a + 5% wt/wt FePO₄ (Aluminium) 1.9 ± 0.9 Adhesive 2a + 5% wt/wt FeCit (Aluminium) 2.6 ± 0.7 Adhesive 2b + 5% wt/wt Na₂CO₃ (Aluminium) 0.9 ± 0.5 Adhesive 2b + 2.5% wt/wt Na₂CO₃ (Aluminium) 1.6 ± 0.9 Adhesive 2b + 5% wt/wt Na₃VO₄ (Aluminium) 1.2 ± 0.6 Adhesive 2b + 2.5% wt/wt Na₃VO₄ (Aluminium) 0.8 ± 0.5 Adhesive 2b + 5% wt/wt Na₃VO₄ (Ceramic) 0.3 ± 0.2 Adhesive 2b + 5% wt/wt TBAP (Aluminium) 1.7 ± 0.5 Adhesive 2b + 2.5% wt/wt TBAP (Aluminium) 0.8 ± 0.3 Adhesive 2b + 5% wt/wt FePO₄ (Aluminium) 0.6 ± 0.3 Adhesive 2a + Adhesive 2b + 5% wt/wt Na₂CO₃ 1.6 ± 0.5 (Aluminium) Adhesive 2a + Adhesive 2b + 5% wt/wt Na₂CO₃ (Glass) 1.9 ± 0.2

TABLE 4b Mechanical properties of bioadhesives on differing substrates tested at room temperature (~22° C.) without crosslinking agents under modified ASTM D905-08 conditions. Data obtained by compression lap shear strength test using an Instron 4301 universal testing machine, with a 1000 N load cell and an applied strain rate of 2 mm/min. Testing was conducted on standard sized samples consisting of two pieces of dry adherends with approximately 0.20 g of adhesive between surfaces. Contact surface areas were kept constant (90 mm²) for all samples in the set. Results are expressed as Mean ± standard deviation, n = 4. Glass is defined as commercially available plain glass slides. Ceramic samples are composed of calcium polyphosphate tablets. Adhesive & Substrate Adhesive Strength (MPa) Adhesive 2a on glass 1.7 ± 0.3 Adhesive 2b on aluminium 1.2 ± 1.0 Adhesive 2b on ceramic 1.6 ± 0.6 Adhesive 2a + Adhesive 2b (50:50 wt %) on glass 1.6 ± 0.2 Adhesive 6 on aluminium ND* Adhesive 6 on glass ND* *ND = No Data; unable to connect to adhesion testing apparatus without premature failure. This is consistent with expected results; i.e., materials without catechol groups are not adhesive.

Without the incorporation of the crosslinking agents (Table 4b), the adhesive strengths of all the adhesives were independent of the substrate employed—a characteristic indicative of the inherent cohesive susceptibility of the uncrosslinked adhesives at the test conditions (room temperature).

Table 4a shows that upon addition of the various crosslinking agents, the adhesion strength of Adhesive 2a could be increased five-fold. On the other hand, Adhesive 2b presented no apparent improvements in its cohesive strength with the use of oxidants or complexing agents (Table 4a). This difference in performance upon crosslinking between the adhesives can be directly linked to their crosslinked glass transition temperatures; recall from Table 3b that upon crosslinking, the Tg of Adhesive 2a moves to above room temperature, whilst that of Adhesive 2b is still well below room temperature. This means that under the adhesion strength test condition, the crosslinked Adhesive 2a is tested in its glassy state, while crosslinked Adhesive 2b is still flowable and thus easily sheared at room temperature. This result teaches that improving adhesion strength/crosslink density with the use of crosslinking agents is strongly dependent on the degree of rigidification that occurs during the curing process and, therefore, on the molecular weights of the adhesive, as was previously discussed in Example 10.

Example 12b: The Effect of Temperature on Adhesive Strength

Adhesives were tested at temperatures above and below their glass transition temperatures in order to determine the influence of temperature on their performance. Glass transition temperatures were determined using dynamic scanning calorimetry (DSC), and adhesion strength was measured using a compressive shear test. Results are reported in Table 4c for non-crosslinked samples.

TABLE 4c Mechanical properties of bioadhesives tested approximately 20° C. above and 20° C. below the midpoint of their glass transition temperature (as determined by DSC) without crosslinking agents on rectangular aluminium stubs under modified ASTM D905-08 conditions. Adhesive mixtures were prepared by cryogenic milling. Approximately 60 mg of the adhesive was applied evenly over the 2 cm² surface area. Testing was conducted after samples stabilized at the required testing temperatures. Data obtained by compression lap shear strength testing using Instron 4301 universal testing machine, with a 1000 N load cell and an applied strain rate of 5.0 mm/min. Results are expressed as Mean ± standard deviation, n = 3. Tg Test Temp Stress (MPa) Adhesive (° C. on heat) [° C.] Above Tg Below Tg Adhesive 2c −40.8 ± 1.5  −80, −20 0.22 ± 0.12 4.38 ± 0.85 Adhesive 3a −8.1 ± 1.4 −80, −10 0.71 ± 0.71 2.24 ± 0.90 Adhesive 5 14.2 ± 3.0 4, 37 1.07 ± 0.47 1.28 ± 0.62 Adhesive 2b −21.5 ± 1.8  −80, 4 0.16 ± 0.08 3.84 ± 1.13 Mixture (wt/wt %)-90 Adhesive 18.0 ± 0.3 4, 37 1.36 ± 0.31 1.54 ± 0.64 5/10 Adhesive 2b Mixture (wt/wt %)-80 Adhesive 11.9 ± 0.6 4, 37 0.92 ± 0.42 1.52 ± 0.91 5/20 Adhesive 2b Mixture (wt/wt %)-70 Adhesive  6.6 ± 2.0 −20, 37 0.87 ± 0.48 1.59 ± 0.08 5/30 Adhesive 2b Mixture (wt/wt %)-60 Adhesive  0.7 ± 2.3 −20, 37 0.48 ± 0.38 1.19 ± 0.51 5/40 Adhesive 2b

Table 4c shows the adhesion strengths of the adhesives at different temperatures. Since no oxidants were used in these experiments to induce crosslinking, the results presented reflect the natural cohesive strengths of the reported dry adhesive formulations. As is typical of all thermoplastic/hotmelt adhesives, the adhesives, without crosslinking, were vulnerable to the temperature at which they were tested, typically presenting higher adhesion strengths at temperatures well below their glass transitions.

In formulations with glass transitions far below 37° C., the adhesive strengths are considerably reduced at room temperature or physiological temperatures, and the adhesives fail cohesively. For example, Adhesive 2a and Adhesive 2b exhibit poor cohesion at simulated physiological temperatures, undergoing flow and creep behaviour when minimal forces are applied. However, when doped with an adhesive with a Tg closer to 37° C. (e.g. Adhesive 5), the glass transitions are shifted towards higher temperatures, allowing these materials to be functional at physiological temperatures, thereby increasing their utility.

Compared to all of the pure adhesives, Adhesive 5 has a uniquely high glass transition temperature which accounts for its high cohesive strengths well above its Tg (at 37° C.) without the necessity for a crosslinking agent. This feature is unique among the many formulations found in the patent literature which require co-oxidants to achieve practical cohesive strength within a finite period under wet conditions. This novel finding capitalizes on uniquely defined thermal transitions that the material undergoes. The polymer is naturally adhesive, even at room temperature.

Example 12c: Testing Adhesion Under Wet Conditions

Compared to the starting oligomers, the adhesives possess increased hydrophilicity on account of the urethane and urea linkages present in the adhesives, in addition to the already existing ester group linkages of the starting oligomers. While these are desirable for biodegradability, these same properties also can make the adhesives susceptible to failure due to water ingress during use.

Possible strategies to reduce water ingress include increasing the hydrophobic domains within the adhesive system by blending with more hydrophobic adhesives and/or additives such as high molecular weight (HMW) PCL, and/or increasing the crosslinking within the adhesive network so as to decrease the swelling potential of the adhesive itself whilst maintaining or improving the cohesive integrity of the system.

To assess the performance of the adhesives for use under surgical conditions, the adhesive strengths of various physically linked and chemically crosslinked adhesive samples were investigated. Adhesive mixtures were cryogenically milled, applied to aluminium stubs, and submerged in simulated body fluid (PBS) at 37° C. for 24 hrs. Adhesion strength was assessed using a compressive shear test. Results are presented in Table 4d alongside the dry strengths of the respective samples (tested at time 0 with equilibration to 37° C. prior to testing).

TABLE 4d Mechanical properties of crosslinked bioadhesives tested at physiological temperatures (37° C.) on rectangular aluminium stubs under modified ASTM D905-08 conditions. Adhesive mixtures were prepared by cryogenic milling. Approximately 60 mg of the adhesive/adhesive blend was applied evenly over the 2 cm² surface area. Samples were submerged in PBS for 24 hrs at 37° C. Data was obtained by compression lap shear strength testing using Instron 4301 universal testing machine, with a 1000 N load cell and an applied strain rate of 5.0 mm/min. Results are expressed as Mean ± standard deviation, n = 4. Dry strength refers to adhesion strength values obtained at 37° C. with no incubation period, and wet strength refers to adhesion strength values obtained after incubation in PBS solution at 37° C. for 24 hrs. Dry Strength Wet Strength Adhesive (MPa) (MPa) Adhesive 2a 1.27 ± 0.51 0.40 ± 0.37 Mixture (wt/wt %)-Adhesive 5:Adhesive 2b, 90:10 1.36 ± 0.30 1.82 ± 0.59 Mixture (wt/wt %)-PCL:Adhesive 2a, 50:50 1.38 ± 0.42 0.19 ± 0.05 Mixture (wt/wt %)-PCL:Adhesive 2a: Na₂CO₃, 50:45:5 2.34 ± 0.54 1.07 ± 0.23 Mixture (wt/wt %)-PCL:Adhesive 2a: Na₂CO₃, 60:35:5 — 0.75 ± 0.20 Mixture (wt/wt %)-PCL:Adhesive 2a: Na₂CO₃, 35:60:5 — 0.64 ± 0.24 Mixture (wt/wt %)-PCL:Adhesive 2a: FeCl₃, 50:45:5 1.03 ± 0.28 0.41 ± 0.18 Mixture (wt/wt %)-PCL:Adhesive 2a: FePO₄, 50:45:5 1.31 ± 0.37 1.33 ± 0.28 Mixture (wt/wt %)-PCL:Adhesive 2a: FeCit, 50:45:5 1.42 ± 0.30 1.66 ± 0.64 Mixture (wt/wt %)-PCL:Adhesive 2a: FeCl₃:Na₂CO₃, 0.98 ± 0.50 0.20 ± 0.06 50:45:2.5:2.5 Mixture (wt/wt %)-PCL:Adhesive 2a: FePO₄:Na₂CO₃, 1.26 ± 0.29 1.30 ± 0.41 50:45:5 Mixture (wt/wt %)-PCL:Adhesive 2a: FeCit:Na₂CO₃, 1.19 ± 0.45  1.5 ± 0.58 50:45:5 Mixture (wt/wt %)-Adhesive 2a:FePO₄, 95:5 1.33 ± 0.37 0.87 ± 0.27 Mixture (wt/wt %)-Adhesive 2a:FeCl₃, 95:5 3.82 ± 0.75 1.23 ± 0.36 Mixture (wt/wt %)-Adhesive 2a:Na₂CO₃, 95:5 1.10 ± 0.30 0.35 ± 0.33 Mixture (wt/wt %)-Adhesive 2a:TBAP, 95:5 1.59 ± 0.21 0.89 ± 0.50

Table 4d shows that for many of the tested non-chemically crosslinked systems, the adhesive strengths, whilst strong in shear at 37° C., failed cohesively after a 24 hr of incubation under wet conditions. Thus, inducing physical chain entanglement networks in adhesive-adhesive blends and/or increasing hydrophobic content alone may not be sufficient for adhesive devices intended for use in wet conditions.

On the other hand, the best strength retention performances were obtained when the adhesives were blended with both PCL and crosslinkers. Without wishing to be bound by a theory, it is possible that the inorganic salts function as both crosslinkers and second phase strengtheners, and PCL is beneficial in wet environments to slow leaching or dissolution of the second phase strengtheners from the adhesive blends.

The effect of neutral soluble (NaCl) and basic insoluble (tricalcium phosphate) salts on the strength retention of the adhesives was further investigated in order to further understand the significance of the crosslinking reactions compared to phase strengthening roles of the inorganic salts. Results are presented in Table 4e.

TABLE 4e Mechanical properties of crosslinked bioadhesives tested at physiological temperatures (37° C.) on rectangular aluminium stubs under modified ASTM D905-08 conditions. Adhesive mixtures were prepared by cryogenic milling. Approximately 50 mg of the adhesive blend was applied (without the aid of heat to induce crosslinking) evenly over the 2 cm2 surface area. Samples were submerged in PBS for 24 hrs at 37° C. Data obtained by compression lap shear strength testing using Instron 4301 universal testing machine, with a 1000 N load cell and an applied strain rate of 5.0 mm/min. Results are expressed as Mean ± standard deviation, n = 4. Additive Wet Strength (MPa) Tricalcium phosphate (TCP) 0.74 ± 0.03 Sodium chloride (NaCl) 0.41 ± 0.28 Sodium carbonate (Na₂CO₃) 1.23 ± 0.27 PCL (control) 0.67 ± 0.14

It was assumed that if phase strengthening alone were responsible for the wet adhesion strengths, then only the insoluble salt (TCP) would have presented any improvements compared to the soluble neutral (NaCl) and basic (Na₂CO₃) salts and the control (PCL). Alternately, if pH-induced crosslinking alone was responsible for the wet adhesion strengths, then both Na₂CO₃ and TCP would present the desired strength retention values. Table 4e, however, shows that neither of these were the case—only the soluble but basic Na₂CO₃ salt presented any significant wet strength retention value. Without wishing to be bound by theory, sodium carbonate may dissolve in the presence of water to increase the local pH surrounding the adhesive, possibly stimulating oxidation of the dopamine residues, thus resulting in pH-induced crosslinking. In the presence of PCL, the adhesive-PCL chain entanglements may facilitate localized pooling of the basic solution, affording the pH-induced crosslinking reaction time to occur.

Overall, these results reinforce the importance of increasing both the crosslinking density and the hydrophobic content within the adhesives in order to improve adhesive strength.

Example 13: Testing Adhesion Under Wet Conditions on Biological Tissues (Bone)

Ideally, bioadhesive devices will function in wet, biofouled conditions at physiological temperatures. Additionally, the adhesives cannot rely on solvent drying for curing and should not be cytotoxic or release cytotoxic degradation products. These are the major challenges of surgical adhesive development. In particular, water ingress and/or solubility is the downfall of many adhesives, especially when they are not fully dry from solvents. The suitability of these adhesives for use in surgical applications was assessed using adhesive tests on samples which were wet or submerged for 24 h. However, submerged samples do not reflect the in vivo environment, but more show the resistance to water ingress. In fact, maintaining strength in vivo may actually prove easier, as there is far less diffusion and available water at the implant.

Example 13a: Water Ingress

Compared to the starting oligomers, the adhesives possess increased hydrophilic domains on account of the urethane and urea linkages present in the adhesives, in addition to the already existing ester group linkages of the starting oligomers. While these are desirable for biodegradability, these same properties also can make the adhesives susceptible to failure due to water ingress during use. To reduce water ingress, high molecular weight (HMW) PCL and sodium carbonate (a cross-linking agent) were combined with the adhesives. HMW PCL increases the hydrophobicity of the adhesive due to the intrinsic hydrophobicity of the PCL itself. Without wishing to be bound by a theory, sodium carbonate may act as both a second phase strengthener and a cross-linker. It will dissolve in the presence of water to increase the local pH surrounding the adhesive, possibly stimulating oxidation of the dopamine residues, thus resulting in crosslinking. This crosslinking could further reduce water ingress and support adhesion. Both additives may not be necessary to prevent ingress, especially because of the low surface area exposed to physiological fluid in vivo; however, both are shown here as proof of principle.

Wet Bone Substrate Preparation

Process of preparing adhesives for the device:

Prior to testing, the adhesives were processed to incorporate different mixtures of specific adhesives or additives. Additives can be oxidants, polymers or second phase strengtheners. Here we combined Adhesive 2a with PCL (˜90 kDa) and Na₂CO₃ at a 35:60:5 ratio, respectively, for protection against water ingress. HMW PCL increases hydrophobicity and Na₂CO₃ provides second-phase strengthening and the possibility for pH induced crosslinking in the event of water ingress. The adhesive mixtures were homogenized by cryo-milling on a Retsch CryoMill (Retsch, Del.) equipped with a 50 mL steel milling jar with 4 steel ball bearings. Samples were cooled to −196° C. using one 10 min precooling cycle prior to 8×5-minute cryomilling cycles at 30 Hz. Adhesive mixtures were allowed to return to room temperature before being removed from the steel milling jar. The finely powdered, homogenized adhesive mixtures were transferred to scintillation flasks using a cooled polyethylene funnel and stored at −20° C. until use.

Flesh was removed from porcine rib bones and the surfaces were washed using aqueous detergent and ethanol to remove fats and residual material. Ribs were submerged in a phosphate buffered saline (PBS, Sigma) and allowed to incubate for at least 5 minutes before testing.

Preparation of Support Material:

PCL sheets were prepared by hot pressing using a Carver laboratory press. 4.6 g of PCL pellets (MW=90,000 g/mol, Sigma) were placed in a stainless-steel mold with a template 15.0×20.0×4×10⁻² cm. The mold was placed on the platen between PTFE liners. Platens were heated to 190° C., and the pellets were heated until translucent. A top sheet was applied to the melt and ˜2 metric tonnes of pressure was applied, pressing the melted polymer pellets into the mold. Locking vice grips were then attached to the plates on three sides to maintain pressure when removing from the press. Full pressure was held for ˜30 s before slowly being released. The template was plunged into a sink filed with cold water to quench the polymer films from the melt. When the plates were cold, the vice grips were removed, and the PCL sheet was carefully removed from the mold. Sheets were trimmed to the mold dimensions with scissors, and further cut into 1.0×4.0 cm strips. An area of 1.5×1.0 cm was marked on each strip for consistent adhesive application. Marked regions on the strips were crimped using vice-grips to increase flexibility and provide a texture. PCL strips were plasma treated for 2 min under a partial oxygen atmosphere using a plasma cleaner (Harrick Plasma, USA) with an attached oxygen tank.

Preparation of Device:

To prepare samples, the adhesive formulation was warmed to room temperature before exposing to atmosphere (preventing condensation). The adhesive formulation was warmed using a forced air, electric heat gun to allow for spreading onto the bone using a spatula. The PCL strip was pressed by hand onto the adhesive for ˜10 s to form the adhesive backing. Wet bones were incubated for 5 minutes in PBS and blotted dry before applying the adhesive. Samples were incubated at 37° C. for 24 h in either air or tap water before testing.

A commercially available, surgical cyanoacrylate-based adhesive was used as a control, but due to some limitations the application protocol was adapted. Bone samples were prepared in the same manner. The adhesive was applied to the wet bone surface and the PCL film was applied to the adhesive. However, due to slow curing of the commercial adhesive, the film was held for up to 5 minutes before moving to incubator. In one case, lab tape was wrapped around the bone to hold the PCL in place while the adhesive cured for 5 minutes. Delamination (due to incomplete curing) was observed on the edge of most samples and additional cyanoacrylate was added to the edges to accommodate.

Samples were loaded mechanically, immediately after removing from the 37° C. environment. Mechanical testing was performed using an Instron 4301 Universal Testing Machine (Instron) with a 200 N load cell and an applied strain rate of 5 mm/min in tensile mode. Samples were clamped ˜1 mm below the tape application site on the bone and 2.5 cm above the bone on the tape side. Tests were finished after failure occurred or yielding in the PCL strip was observed. Failure mechanism was recorded by visual inspection after failure.

TABLE 5a Mechanical properties of an adhesive blend (Adhesive 2a:PCL (~90 kDa):Na₂CO₃ at a 35:60:5 w/w ratio) obtained by modified lap shear testing using Instron 4301 universal testing machine, with a 200 N load cell and an applied strain rate of 5 mm/min. Results are shown as means ± standard deviations and are reported for the adhesive blend on dry (uncrosslinked), PBS wetted (induced crosslinking) and submerged porcine bone (induced crosslinking), compared to a commercially available surgical cyanoacrylate (Covidien surgical adhesive). Asterisks indicate the number of adhesive failures. Sample Condition Peak Force [N] Peak Stress [kPa] N value Dry bone 52.82 ± 6.87 264.08 ± 34.36 n = 3; 3* PBS-Wetted bone 46.97 ± 3.09 234.86 ± 15.46 n = 3; 1* Submerged bone (in water)  44.07 ± 24.42  220.34 ± 122.10 n = 8 Wet bone-cyanoacrylate 67.90 ± 6.70 339.52 ± 33.51 n = 3

No significant difference was observed between the dry, wet and submerged bone samples using ANOVA analysis, indicating that the inclusion of the hydrophobic PCL segments and/or pH-induced crosslinking were effective for preventing/reducing water ingress within the adhesives upon use.

In all conditions, most failures occurred in the PCL film, and were observed as necking occurring at the tape region which did not overlap the bone with a resulting drop in the observed stress. Where failures did not occur in the tape region, the systems failed adhesively, as indicated by the asterisks in the table above. These results show that the cohesive integrity of the adhesive systems remained intact when used under wet conditions (i.e., on wet systems and upon submersion).

Further, the tested adhesive performed as well as commercial, surgical cyanoacrylate even after being submerged for 24 h, indicating the commercial suitability of the adhesive formulations presented herein. A further advantage of the claimed adhesives compared to commercial counterparts such as that used herein is the ease of use; as reported above, the commercial adhesive was very slow curing, and required extra effort and time to keep the adherends in position while the adhesive set. On the other hand, the claimed adhesives of this work ‘set’ immediately upon heat spreading/contact.

Example 13b: Testing Effect of Physiological Fluids on Adhesion

To test the effect of physiological fluids on adhesion of a polymer film to bone, tensile tests were conducted on samples submerged in varying solutions for 24 h.

Adhesive was prepared by combining Adhesive 2a with PCL (˜90 kDa) and Na₂CO₃ at a 35:60:5 ratio, respectively, as described above. Adhesive was applied to the bone and gently heated using a heat lamp. PCL (90 kDa) film was cut into 1×4 cm pieces, crimped and plasma treated before application. The strips were applied to warm bone-adhesive samples and pressed for ˜10 s. The overlap area was held constant at ˜2 cm². Samples were submerged in water (control), PBS and equine blood (void of clotting factors) and incubated at 37° C. for ˜24 h. After incubation, samples were rinsed with ultrapure water and held at 37° C. until testing.

Samples were loaded mechanically, immediately after removing from the 37° C. environment. Mechanical testing was performed using an Instron 4301 Universal Testing Machine (Instron) with a 100 N load cell and an applied strain rate of 5 mm/min in tensile mode. Samples were clamped ˜1 mm below the tape application site on the bone and 2.5 cm above the bone on the tape side. Tests were finished after failure occurred or yielding in the PCL strip was observed. Failure mechanism was recorded by visual inspection after failure.

Data analysis was performed with IBM SPSS Statistics version 25.0. One-way ANOVA and Tukey post-hoc tests were used to analyze data comparing the different physiological solutions. The level of significance was set at 5%.

TAB:E 5b Adhesive strength values of polymer film with Adhesive 2a combined with PCL and Na₂CO₃ (35:60:5 ratio) to bone submerged in different physiological solutions. Data was generated in a tensile test at a strain rate of 5 mm/min with an overlap area of 2 cm². Results are shown as mean ± standard deviation (n = 3). Sample Condition Peak Force [N] Peak Stress [kPa] N value Water  41.03 ± 11.05 ab  205.16 ± 55.29 ab 3 PBS 37.73 ± 15.07 b 172.04 ± 46.74 b 3 Blood 56.41 ± 3.20 a  282.06 ± 15.99 a 3

No statistical significance was found between the peak force values for samples incubated in water and PBS, while samples incubated in blood exhibited significantly higher values (Table 5).

All samples submerged in water and PBS failed adhesively whereas two of the three samples incubated in blood failed within the tape (observed as necking occurring at the tape region which did not overlap the bone, similar to what was presented in Example 13a).

The bar graph (FIG. 31 ) shows the failure modes for the samples incubated in physiological fluids for 24 h. All sample preparation was done in a similar manner. Evidently, higher failure forces exhibited by samples incubated in blood are consistent with both stronger cohesive and adhesive performance of the adhesives under simulated real-use conditions.

Example 14: Testing Effect of Residual Solvent on Adhesive Performance

Residual solvent is a major challenge for bioadhesives. Synthesis in the presence of a solvent requires rigorous drying protocols to fully remove solvent, as solvents are often cytotoxic, and could accelerate in water ingress.

To test the effect of residual solvent on mechanical properties of uncrosslinked adhesive increasing amounts of solvent were incorporated into adhesive and mechanical properties were measured using a modified lap shear test. This experiment was designed to mimic both incomplete drying of the adhesive after synthesis, and what occurs when solvents are utilized for adhesive spreading and/or adhesive application.

To incorporate increasing amounts of solvent into adhesives, the process started with dry Adhesive 5. Using cryogenic milling 0, 5, 10 and 50 wt % anhydrous ethanol were incorporated into aliquots of adhesive. Briefly, ethanol was added dropwise to a specific mass percent of the adhesive. Adhesive/solvent mixtures were added to a large 50 mL steel milling canister containing 4 ball-bearings. Adhesive/ethanol mixtures were homogenized using cryogenic milling on a Retsch cryomill at −196° C. Mixtures were milled for 3 cycles at 30 Hz with ˜5 minutes of cooling between cycles. Adhesive-ethanol mixtures were transferred to scintillation vials and stored at −20° C. before use.

Aluminum stubs were prepared and cleaned with acetone. The surface of each stub was smooth, and a 2×1 cm area was indicated to ensure constant overlap area. ˜60 mg of each adhesive-ethanol mixture was spread onto the stubs and an overlapping stub was applied by hand and pressed together for ˜10 s. 0 and 5 wt % ethanol adhesives required some heat for spreading. Overlap area was held constant at 2 cm². Values could not be obtained for 50 wt % ethanol adhesive, as the cohesive strength was insufficient to hold the aluminum stubs together. Even at 10 wt % ethanol, the adhesive exhibited insufficient strength; the force of gravity resulted in deformation. 4 repeats of 0, 5, and 10 wt % ethanol adhesives were prepared and kept at room temperature for ˜1 hr before testing.

Samples were tested on a Universal Testing Machine (Instron) under compression, using a modified lap shear test, at a strain rate of 5 mm/min. Stress and displacement data were recorded.

Increasing amounts of residual ethanol affected the cohesive strength of Adhesive 5. FIG. 32 shows adhesive strength with increasing residual solvent. 5 wt % ethanol reduced adhesive strength by 9×. Data was generated in compression using a modified lap shear test at a strain rate of 5 mm/min on aluminum stubs with an overlap area of 2 cm². Samples were tested at room temperature. Error bars indicate standard deviation (n=4). Doubling solvent to 10 wt % further reduced adhesive strength by ˜30×.

Clearly, increasing amounts of residual solvent decreases the cohesive strength of adhesives.

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1. A water insoluble adhesive comprising: a compound of structure 1

Structure I wherein the compound has a Tg lower than 25° C.; the compound is water insoluble; B is a branched or unbranched oligomer derived from a polyester, polyether, polyalkylene glycol, polysilicone or polycarbonate with a MW<10,000 g/mol; Linker L is an urethane, urea bond, or amide bond; Linker L′ is an urethane or urea bond; A is a chain extender of Mw 3000 g/mol comprising substituted or unsubstituted alkyl, cycloalkyl and/or aromatic groups; W is a terminal adhesive selected from an adhesive benzene-1,2-diol derivative or an adhesive benzene-1,2,3-triol derivative; m is 0 or 1; and n is 0, 1, 2, 3 or 4; or a cross-linked polymer produced by cross-linking compounds of structure
 1. 2. The water insoluble adhesive of claim 1, wherein m is 1 and the adhesive comprises a compound of structure 2

Structure 2 or a cross-linked polymer produced by cross-linking compounds of structure
 2. 3. The water insoluble adhesive of claim 2 wherein n is 0 and the adhesive comprises a compound of structure 3

Structure 3 or a cross-linked polymer produced by cross-linking compounds of structure 3 or n is 1 and the adhesive comprises a compound of structure 4

Structure 4 or a cross-linked polymer produced by cross-linking compounds of structure 4, or n is 2 and the adhesive comprises a compound of structure 5

Structure 5 or a cross-linked polymer produced by cross-linking compounds of structure 5, or. n is 3 and the adhesive comprises a compound of structure 6

Structure 6 or a cross-linked polymer produced by cross-linking compounds of structure 6, or n is 4 and the adhesive comprises a compound of structure 7

Structure 7 or a cross-linked polymer produced by cross-linking compounds of structure
 7. 4-7. (canceled)
 8. The water insoluble adhesive of claim 1 wherein the compound has a Tm equal to or greater than 37° C.
 9. The water insoluble adhesive of claim 1, wherein B has a Mw<5,000 g/mol and/or is hydrolysable or enzyme degradable.
 10. (canceled)
 11. The water insoluble adhesive of claim 1, wherein L and/or L′ is hydrolysable or enzyme degradable.
 12. The water insoluble adhesive of claim 1, wherein B is an oligomer derived from polycaprolactone, polydimethylsiloxane, polypropylene glycol or polyhexamethylene carbonate.
 13. The water insoluble adhesive of claim 1, wherein A is a substituted or unsubstituted alkyl group and/or has a MW<200 g/mol. 14-16. (canceled)
 17. The water insoluble adhesive of claim 1, wherein W has a structure selected from:

wherein R is present or absent and when present is a C1-C6 alkyl group or C1-C6 alkene optionally substituted with OH, NH. 18-21. (canceled)
 22. The water insoluble adhesive of claim 1, wherein the adhesive comprises a compound of structure 1 and a cross-linking agent. 23-28. (canceled)
 29. The water insoluble adhesive of claim 1 having an adhesive strength greater than 25 KPa under compression, tensile, or tensile lap shear testing. 30-31. (canceled)
 32. The water insoluble adhesive of claim 1, wherein the adhesive has free-flowing behavior at a temperature of at least 20° C.
 33. (canceled)
 34. (canceled)
 35. A method of adhering a first surface and a second surface comprising: applying the adhesive of claim 1 to at least a portion of the first surface; and bringing at least a portion of the second surface into contact with the adhesive.
 36. (canceled)
 37. The method of claim 35 wherein at least one of the surfaces is a wet surface, saline surface and/or a surface contaminated with proteins and/or biomolecules.
 38. The method of claim 35, wherein the first surface comprises soft tissue and the second surface comprises hard tissue or an implant or device or the first surface and the second surface or the first surface comprises hard tissue and the second surface is a surface of an implant or device are soft tissue or the first surface and the second surface are hard tissue. 39-41. (canceled)
 42. A method of adhering a substance to blood or components thereof comprising contacting the substance and the blood or components thereof with an adhesive according to claim
 1. 43. (canceled)
 44. The adhesive of claim 2 wherein the compound is prepared by reacting a first isocyanate group of a diisocyanate having a substituted or unsubstituted alkyl-derived chain extender, a substituted or unsubstituted cycloalkyl-derived chain extender, or a substituted or unsubstituted benzyl-derived chain extender between the two isocyanate groups with terminal amino or alcohol groups of an oligomer having at least two terminal amino or alcohol groups and reacting a second isocyanate of the diisocyanate molecule with an amine group, alcohol group or carboxy group present on an alkyl chain of a 4-alkylbenzene-1,2-diol derivative or a 5-alkylbenzene-1,2,3-triol derivative.
 45. The adhesive of claim 44 wherein the oligomer is an oligomer derived from a polyester, polyether, polyalkyloxide, polysilicone or polycarbonate.
 46. (canceled)
 47. The adhesive of claim 44, wherein the diisocyanate molecule is selected from the group consisting of:


48. The adhesive of claim 44, wherein the 4-alkylbenzene-1,2-diol derivative or a 5-alkylbenzene-1,2,3-triol derivative is selected from the group consisting of: 